-
1
-
-
0027204584
-
All known human H1 histone genes except the H1 gene are clustered on chromosome 6
-
1. Albig, W., Drabent, B., Kunz, J., Kalff-Suske, M., Grzeschik, K-H., and Doenecke, D. (1993). All known human H1 histone genes except the H1 gene are clustered on chromosome 6. Genomics 16: 649-654.
-
(1993)
Genomics
, vol.16
, pp. 649-654
-
-
Albig, W.1
Drabent, B.2
Kunz, J.3
Kalff-Suske, M.4
Grzeschik, K.-H.5
Doenecke, D.6
-
2
-
-
0021760639
-
The isolation of a human Ig Vλ, gene from a recombinant library of chromosome 22 and estimation of its copy number
-
2. Anderson, M. L. M., Szajnert, M. F., Kaplan, J. C., McColl, L., and Young, B. D. (1984). The isolation of a human Ig Vλ, gene from a recombinant library of chromosome 22 and estimation of its copy number. Nucleic Acids Res 12: 6647-6660.
-
(1984)
Nucleic Acids Res
, vol.12
, pp. 6647-6660
-
-
Anderson, M.L.M.1
Szajnert, M.F.2
Kaplan, J.C.3
McColl, L.4
Young, B.D.5
-
3
-
-
0028125576
-
Cloning of the cDNA encoding human tissue inhibitor of metalloproteinases-3 (TIMP-3) and mapping of the TIMP-3 gene to chromosome 22
-
3. Apte, S. S., Mattei, M. G., and Olsen, B. R. (1994). Cloning of the cDNA encoding human tissue inhibitor of metalloproteinases-3 (TIMP-3) and mapping of the TIMP-3 gene to chromosome 22. Genomics 19: 86-90.
-
(1994)
Genomics
, vol.19
, pp. 86-90
-
-
Apte, S.S.1
Mattei, M.G.2
Olsen, B.R.3
-
4
-
-
0026674402
-
Localization of the t(2;13) breakpoint of alveolar rhabdomyosarcoma on a physical map of chromosome 2
-
4. Barr, F. G., Holick, J., Nycum, L., Biegel, J. A., and Emanuel, B. S. (1992). Localization of the t(2;13) breakpoint of alveolar rhabdomyosarcoma on a physical map of chromosome 2. Genomics 13: 1150-1156.
-
(1992)
Genomics
, vol.13
, pp. 1150-1156
-
-
Barr, F.G.1
Holick, J.2
Nycum, L.3
Biegel, J.A.4
Emanuel, B.S.5
-
5
-
-
0027953313
-
The E subunit of vacuolar H(+)-ATPase localizes close to the centromere on human chromosome 22
-
5. Baud, V., Mears, A. J., Lamour, V., Scamps, C., Duncan, A. M., McDermid, H. E., and Lipinski, M. (1994). The E subunit of vacuolar H(+)-ATPase localizes close to the centromere on human chromosome 22. Hum. Mol. Genet. 3: 335-339.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 335-339
-
-
Baud, V.1
Mears, A.J.2
Lamour, V.3
Scamps, C.4
Duncan, A.M.5
McDermid, H.E.6
Lipinski, M.7
-
6
-
-
0022764276
-
Characterization of a group of transposed human V kappa genes
-
6. Bauer, H. G., Pech, M., and Zachau, H. G. (1986). Characterization of a group of transposed human V kappa genes. Biol. Chem. Hoppe-Seyler 367: 751-755.
-
(1986)
Biol. Chem. Hoppe-seyler
, vol.367
, pp. 751-755
-
-
Bauer, H.G.1
Pech, M.2
Zachau, H.G.3
-
7
-
-
0027494505
-
Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2
-
7. Bauer, T. R., McDermid, H. E., Budarf, M. L., Van Keuren, M. L., and Blomberg, B. B. (1993). Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2. Immunogenetics 38: 387-399.
-
(1993)
Immunogenetics
, vol.38
, pp. 387-399
-
-
Bauer, T.R.1
McDermid, H.E.2
Budarf, M.L.3
Van Keuren, M.L.4
Blomberg, B.B.5
-
8
-
-
0028814128
-
Integration of physical, breakpoint and genetic maps of chromosome 22. Localization of 587 yeast artificial chromosomes with 238 mapped markers
-
8. Bell, C. J., Budarf, M. L., Nieuwenhuijsen, B. W., Barnoski, B. B., Buetow, K. H., Campbell, K., Colbert, A., Collins, J., Desjardins, P. R., DeZwaan, T., Eckman, B., Foote, S., Hart, K., Hiester, K., Van Het Hoog, M. J., Hopper, E., Kaufman, A., McDermid, H. E., Overton, G. C., Reeve, M. P., Searls, D. B., Stein, L., Valmiki, V. H., Watson, E., Williams, S., Winston, R., Nussbaum, R. L., Lander, E. S., Fischbeck, K., Emanuel, B. S., and Hudson, T. J. (1995). Integration of physical, breakpoint and genetic maps of chromosome 22. Localization of 587 yeast artificial chromosomes with 238 mapped markers. Hum. Mol. Genet. 4: 59-69.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 59-69
-
-
Bell, C.J.1
Budarf, M.L.2
Nieuwenhuijsen, B.W.3
Barnoski, B.B.4
Buetow, K.H.5
Campbell, K.6
Colbert, A.7
Collins, J.8
Desjardins, P.R.9
DeZwaan, T.10
Eckman, B.11
Foote, S.12
Hart, K.13
Hiester, K.14
Van Het Hoog, M.J.15
Hopper, E.16
Kaufman, A.17
McDermid, H.E.18
Overton, G.C.19
Reeve, M.P.20
Searls, D.B.21
Stein, L.22
Valmiki, V.H.23
Watson, E.24
Williams, S.25
Winston, R.26
Nussbaum, R.L.27
Lander, E.S.28
Fischbeck, K.29
Emanuel, B.S.30
Hudson, T.J.31
more..
-
9
-
-
0026034792
-
Human catechol-O-methyl-transferase: Cloning and expression of the membrane-associated form
-
9. Bertocci, B., Miggiano, V., Da Prada, M., Dembic, Z., Lahm, H. W., and Malherbe, P. (1991). Human catechol-O-methyl-transferase: Cloning and expression of the membrane-associated form. Proc. Natl. Acad. Sci. USA 88: 1416-1420.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 1416-1420
-
-
Bertocci, B.1
Miggiano, V.2
Da Prada, M.3
Dembic, Z.4
Lahm, H.W.5
Malherbe, P.6
-
10
-
-
0024450870
-
Monosomy 22 in rhabdoid or atypical teratoid tumors of the brain
-
10. Biegel, J. B., Rorke, L. B., and Emanuel, B. S. (1989). Monosomy 22 in rhabdoid or atypical teratoid tumors of the brain. N. Engl. J. Med. 321: 906.
-
(1989)
N. Engl. J. Med.
, vol.321
, pp. 906
-
-
Biegel, J.B.1
Rorke, L.B.2
Emanuel, B.S.3
-
11
-
-
0022000776
-
A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA
-
11. Bird, A., Taggart, M., Frommer, M., Miller, O. J., and Macleod, D. (1985). A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA. Cell 40: 91-99.
-
(1985)
Cell
, vol.40
, pp. 91-99
-
-
Bird, A.1
Taggart, M.2
Frommer, M.3
Miller, O.J.4
Macleod, D.5
-
12
-
-
0024297509
-
Heparin cofactor II: cDNA sequence, chromosome localization, restriction fragment length polymorphism, and expression in Escherichia coli
-
12. Blinder, M. A., Marasa, J. C., Reynolds, C. H., Deaven, L. L., and Tollefsen, D. M. (1988). Heparin cofactor II: cDNA sequence, chromosome localization, restriction fragment length polymorphism, and expression in Escherichia coli. Biochemistry 27: 752-759.
-
(1988)
Biochemistry
, vol.27
, pp. 752-759
-
-
Blinder, M.A.1
Marasa, J.C.2
Reynolds, C.H.3
Deaven, L.L.4
Tollefsen, D.M.5
-
13
-
-
0027209521
-
Comparative mapping of 9 human chromosome 22q loci in the laboratory mouse
-
13. Bucan, M., Gatalica, B., Nolan, P., Chung, A., Leroux, A., Grossman, M. H., Nadeau, J. H., Emanuel, B. S., and Budarf, M. (1993). Comparative mapping of 9 human chromosome 22q loci in the laboratory mouse. Hum. Mol. Genet. 2: 1245-1252.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1245-1252
-
-
Bucan, M.1
Gatalica, B.2
Nolan, P.3
Chung, A.4
Leroux, A.5
Grossman, M.H.6
Nadeau, J.H.7
Emanuel, B.S.8
Budarf, M.9
-
14
-
-
0024066611
-
Linear order of the four BCR-related loci in 22q11
-
14. Budarf, M., Canaani, E., and Emanuel, B. S. (1988). Linear order of the four BCR-related loci in 22q11. Genomics 3: 168-171.
-
(1988)
Genomics
, vol.3
, pp. 168-171
-
-
Budarf, M.1
Canaani, E.2
Emanuel, B.S.3
-
15
-
-
0024344911
-
Comparative mapping of the constitutional and tumor associated 11;22 translocations
-
15. Budarf, M. L., Sellinger, B., Griffin, C., and Emanuel, B. S. (1989a). Comparative mapping of the constitutional and tumor associated 11;22 translocations. Am. J. Hum. Genet. 45: 128-139.
-
(1989)
Am. J. Hum. Genet.
, vol.45
, pp. 128-139
-
-
Budarf, M.L.1
Sellinger, B.2
Griffin, C.3
Emanuel, B.S.4
-
16
-
-
0024789926
-
Human differentiation-stimulating factor (leukemia inhibitory factor, human interleukin DA) gene maps distal to the Ewing sarcoma breakpoint on 22q
-
16. Budarf, M., Emanuel, B. S., Mohandas, T., Goeddel, D. V., and Lowe, D. G. (1989b). Human differentiation-stimulating factor (leukemia inhibitory factor, human interleukin DA) gene maps distal to the Ewing sarcoma breakpoint on 22q. Cytogenet. Cell Genet. 52: 19-22.
-
(1989)
Cytogenet. Cell Genet.
, vol.52
, pp. 19-22
-
-
Budarf, M.1
Emanuel, B.S.2
Mohandas, T.3
Goeddel, D.V.4
Lowe, D.G.5
-
17
-
-
0025871057
-
Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22
-
17. Budarf, M. L., McDermid, H. E., Sellinger, B., and Emanuel, B. S. (1991a). Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22. Genomics 10: 996-1002.
-
(1991)
Genomics
, vol.10
, pp. 996-1002
-
-
Budarf, M.L.1
McDermid, H.E.2
Sellinger, B.3
Emanuel, B.S.4
-
18
-
-
5244329372
-
Regional sublocalization of the human parvalbumin gene to 22q12 → 13.1
-
18. Budarf, M. L., Collins, J., Ritzler, M., Berchtold, M. W., and Emanuel, B. S. (1991b). Regional sublocalization of the human parvalbumin gene to 22q12 → 13.1. Cytogenet. Cell Genet. 58: 2046.
-
(1991)
Cytogenet. Cell Genet.
, vol.58
, pp. 2046
-
-
Budarf, M.L.1
Collins, J.2
Ritzler, M.3
Berchtold, M.W.4
Emanuel, B.S.5
-
19
-
-
0011976169
-
Isolation and characterization of a cDNA from 22q11.2 that maps to the DiGeorge syndrome critical region (DGCR)
-
19. Budarf, M. L., Baldwin, S., Biegel, J., McDermid, H., Emanuel, B. S., and Driscoll, D. (1992). Isolation and characterization of a cDNA from 22q11.2 that maps to the DiGeorge syndrome critical region (DGCR). Am. J. Hum. Genet. 51: A119.
-
(1992)
Am. J. Hum. Genet.
, vol.51
-
-
Budarf, M.L.1
Baldwin, S.2
Biegel, J.3
McDermid, H.4
Emanuel, B.S.5
Driscoll, D.6
-
20
-
-
0028926898
-
Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/ Velo-cardio-facial chromosomal region in 22q11.2
-
20. Budarf, M. L., Konkle, B. A., Ludlow, L. B., Michaud, D., Li, M., Yamashiro, D. J., McDonald-McGinn, D., Zackai, E. H., and Driscoll, D. A. (1995a). Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/ Velo-cardio-facial chromosomal region in 22q11.2. Hum. Mol. Genet. 4: 763-766.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 763-766
-
-
Budarf, M.L.1
Konkle, B.A.2
Ludlow, L.B.3
Michaud, D.4
Li, M.5
Yamashiro, D.J.6
McDonald-McGinn, D.7
Zackai, E.H.8
Driscoll, D.A.9
-
21
-
-
0028988727
-
Assignment of the human hipoocampal inward rectifier potassium channel (HIR) gene to 22q13.1
-
21. Budarf, M. L., Perier, F., Barnoski, B. L., Bell, C. J., and Vandenberg, C. A. (1995b). Assignment of the human hipoocampal inward rectifier potassium channel (HIR) gene to 22q13.1. Genomics 26: 625-629.
-
(1995)
Genomics
, vol.26
, pp. 625-629
-
-
Budarf, M.L.1
Perier, F.2
Barnoski, B.L.3
Bell, C.J.4
Vandenberg, C.A.5
-
22
-
-
0028998317
-
Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene
-
22. Budarf, M. L., Collins, J., Gong, W., Roe, B., Wang, Z., Sellinger, B., Michaud, D., Driscoll, D., and Emanuel, B. S. (1995c). Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene. Nature Genet. 10: 269-277.
-
(1995)
Nature Genet.
, vol.10
, pp. 269-277
-
-
Budarf, M.L.1
Collins, J.2
Gong, W.3
Roe, B.4
Wang, Z.5
Sellinger, B.6
Michaud, D.7
Driscoll, D.8
Emanuel, B.S.9
-
23
-
-
0027501055
-
A microsatellite-based multipoint index map of human chromosome 22
-
23. Buetow, K. H., Duggan, D., Yang, B., Ludwigsen, S., Puck, J., Porter, J., Budarf, M., Spielman, R., and Emanuel, B. S. (1993). A microsatellite-based multipoint index map of human chromosome 22. Genomics 18: 329-339.
-
(1993)
Genomics
, vol.18
, pp. 329-339
-
-
Buetow, K.H.1
Duggan, D.2
Yang, B.3
Ludwigsen, S.4
Puck, J.5
Porter, J.6
Budarf, M.7
Spielman, R.8
Emanuel, B.S.9
-
24
-
-
0025080192
-
Localization of 2 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome
-
24. Carey, A. H., Roach, S., Williamson, R., Dumanski, J. P., Nordenskjold, M., Collins, V. P., Rouleau, G., Blin, B., Jalbert, P., and Scambler, P. J. (1990). Localization of 2 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome. Genomics 7: 299-306.
-
(1990)
Genomics
, vol.7
, pp. 299-306
-
-
Carey, A.H.1
Roach, S.2
Williamson, R.3
Dumanski, J.P.4
Nordenskjold, M.5
Collins, V.P.6
Rouleau, G.7
Blin, B.8
Jalbert, P.9
Scambler, P.J.10
-
25
-
-
0026688328
-
Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome
-
25. Carey, A. H., Kelley, D., Halford, S., Wade, S., Wilson, D., Goodship, J., Burn, J., Paul, T., Sharkey, A., Dumanski, J., Nordenskjold, M., Williamson, R., and Scambler, P. J. (1992). Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome. Am. J. Hum. Genet. 51: 964-970.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 964-970
-
-
Carey, A.H.1
Kelley, D.2
Halford, S.3
Wade, S.4
Wilson, D.5
Goodship, J.6
Burn, J.7
Paul, T.8
Sharkey, A.9
Dumanski, J.10
Nordenskjold, M.11
Williamson, R.12
Scambler, P.J.13
-
26
-
-
0026700321
-
The human "peripheral-type" benzodiazepine receptor: Regional mapping of the gene and characterization of the receptor expressed from cDNA
-
26. Chang, Y. J., McCabe, R. T., Rennert, H., Budarf, M. L., Sayegh, R., Emanuel, B. S., Skolnick, P., and Strauss, J. F. (1991). The human "peripheral-type" benzodiazepine receptor: Regional mapping of the gene and characterization of the receptor expressed from cDNA. DNA Cell Biol. 11: 471-480.
-
(1991)
DNA Cell Biol.
, vol.11
, pp. 471-480
-
-
Chang, Y.J.1
McCabe, R.T.2
Rennert, H.3
Budarf, M.L.4
Sayegh, R.5
Emanuel, B.S.6
Skolnick, P.7
Strauss, J.F.8
-
28
-
-
0021266088
-
Transformation of NIH 3T3 cells by a human c-sis cDNA clone
-
28. Clarke, M. F., Westlin, E., Schmidt, D., Josephs, S. F., Ratner, L., Wong-Staal, F., Gallo, R. C., and Reitz, M. S., Jr. (1984). Transformation of NIH 3T3 cells by a human c-sis cDNA clone. Nature 308: 464-467.
-
(1984)
Nature
, vol.308
, pp. 464-467
-
-
Clarke, M.F.1
Westlin, E.2
Schmidt, D.3
Josephs, S.F.4
Ratner, L.5
Wong-Staal, F.6
Gallo, R.C.7
Reitz, M.S.8
-
29
-
-
0027083352
-
A panel of human chromosome 22-specific sequence tagged sites
-
29. Collins, J. E., Everett, L. A., Bentley, D. R., and Dunham, I. (1992). A panel of human chromosome 22-specific sequence tagged sites. Genomics 14: 1098-1103.
-
(1992)
Genomics
, vol.14
, pp. 1098-1103
-
-
Collins, J.E.1
Everett, L.A.2
Bentley, D.R.3
Dunham, I.4
-
30
-
-
0029653651
-
A high-density YAC contig map of human chromosome 22
-
30. Collins, J. E., Cole, C. G., Smink, L. J., Garrett, C. L., Leversha, M. A., Soderlund, C. A., Maslen, G. L., Everett, L. A., Rice, K. M., Coffey, A. J., Gregory, S. G., Gwilliam, R., Dunham, A., Davies, A. F., Hassock, S., Todd, C. M., Lehrach, H., Hulsebos, T. J. M., Weissenbach, J., Morrow, B., Kucherlapati, R. S., Wadey, R., Scambler, P. J., Kim, U-J., Simon, M. I., Peyrard, M., Xie, Y-G., Carter, N. P., Durbin, R., Dumanski, J. P., Bentley, D. R., and Dunham, I. (1995). A high-density YAC contig map of human chromosome 22. Nature 377: 367-379.
-
(1995)
Nature
, vol.377
, pp. 367-379
-
-
Collins, J.E.1
Cole, C.G.2
Smink, L.J.3
Garrett, C.L.4
Leversha, M.A.5
Soderlund, C.A.6
Maslen, G.L.7
Everett, L.A.8
Rice, K.M.9
Coffey, A.J.10
Gregory, S.G.11
Gwilliam, R.12
Dunham, A.13
Davies, A.F.14
Hassock, S.15
Todd, C.M.16
Lehrach, H.17
Hulsebos, T.J.M.18
Weissenbach, J.19
Morrow, B.20
Kucherlapati, R.S.21
Wadey, R.22
Scambler, P.J.23
Kim, U.-J.24
Simon, M.I.25
Peyrard, M.26
Xie, Y.-G.27
Carter, N.P.28
Durbin, R.29
Dumanski, J.P.30
Bentley, D.R.31
Dunham, I.32
more..
-
31
-
-
0027942568
-
Généthon
-
Weissenbach, J., Gyapay, G., Dib, C., Morrissette, J., Lathrop, G. M., Vignal, A.; University of Utah: White, R., Matsunami, N., Gerken, S., Melis, R., Albertsen, H., Plaetke, R., Odelberg, S.; Yale University: Ward, D.; Centre d'Etude du Polymorphism Humain (CEPH): Dausset, J., Cohen, D., and Cann, H. A comprehensive human linkage map with centimorgan density.
-
31. Cooperative Human Linkage Center (CHLC): Murray, J. C., Buetow, K. H., Weber, J. L., Ludwigsen, S., Scherpbier-Heddema, T., Manion, F., Quillen, J., Sheffield, V. C., Sunden, S., Duyk, G. M.; Généthon: Weissenbach, J., Gyapay, G., Dib, C., Morrissette, J., Lathrop, G. M., Vignal, A.; University of Utah: White, R., Matsunami, N., Gerken, S., Melis, R., Albertsen, H., Plaetke, R., Odelberg, S.; Yale University: Ward, D.; Centre d'Etude du Polymorphism Humain (CEPH): Dausset, J., Cohen, D., and Cann, H. (1994). A comprehensive human linkage map with centimorgan density. Science 265: 2049-2054.
-
(1994)
Science
, vol.265
, pp. 2049-2054
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Scherpbier-Heddema, T.5
Manion, F.6
Quillen, J.7
Sheffield, V.C.8
Sunden, S.9
Duyk, G.M.10
-
32
-
-
0021061389
-
Transcriptional activation of an unrearranged and untranslocated c-myc oncogene by translocation of a Cl locus in Burkitt lymphoma cells
-
32. Croce, C. M., Thierfelder, W., Erikson, J., Nishikura, K., Finan, J., Lenoir, G. M., and Nowell, P. C. (1983). Transcriptional activation of an unrearranged and untranslocated c-myc oncogene by translocation of a Cl locus in Burkitt lymphoma cells. Proc. Natl. Acad. Sci. USA 80: 6922-6926.
-
(1983)
Proc. Natl. Acad. Sci. USA
, vol.80
, pp. 6922-6926
-
-
Croce, C.M.1
Thierfelder, W.2
Erikson, J.3
Nishikura, K.4
Finan, J.5
Lenoir, G.M.6
Nowell, P.C.7
-
33
-
-
2542512686
-
Mapping of the four distinct BCR-related loci to chromosome region 22q11: Order of BCR loci relative to chronic myelogeneous leukemia and acute lymphoblastic leukemia breakpoints
-
33. Croce, C. M., Huebner, K., Isobe, M., Fainstein, E., Lifshitz, B., Shtivelman, E., and Canaani, E. (1987). Mapping of the four distinct BCR-related loci to chromosome region 22q11: Order of BCR loci relative to chronic myelogeneous leukemia and acute lymphoblastic leukemia breakpoints. Proc. Natl. Acad. Sci. USA 84: 7174-7178.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 7174-7178
-
-
Croce, C.M.1
Huebner, K.2
Isobe, M.3
Fainstein, E.4
Lifshitz, B.5
Shtivelman, E.6
Canaani, E.7
-
34
-
-
0025974896
-
Mapping of human chromosome 22 with a panel of somatic cell hybrids
-
34. Delattre, O., Azambuja, C. J., Aurias, A., Zucman, J., Peter, M., Zhang, F., Hors-Cayla, M. C., Rouleau, G., and Thomas, G. (1991). Mapping of human chromosome 22 with a panel of somatic cell hybrids. Genomics 9: 721-727.
-
(1991)
Genomics
, vol.9
, pp. 721-727
-
-
Delattre, O.1
Azambuja, C.J.2
Aurias, A.3
Zucman, J.4
Peter, M.5
Zhang, F.6
Hors-Cayla, M.C.7
Rouleau, G.8
Thomas, G.9
-
35
-
-
0026750771
-
A genetic etiology for DiGeorge syndrome: Consistent deletions and microdeletions of 22q11
-
35. Driscoll, D. A., Budarf, M. L., and Emanuel, B. S. (1992a). A genetic etiology for DiGeorge syndrome: Consistent deletions and microdeletions of 22q11. Am. J. Hum. Genet. 50: 924-933.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 924-933
-
-
Driscoll, D.A.1
Budarf, M.L.2
Emanuel, B.S.3
-
36
-
-
0026662962
-
Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
-
36. Driscoll, D. A., Spinner, N. B., Budarf, M. L., McDonald-McGinn, D. M., Zackai, E. H., Goldberg, R. B., Shprintzen, R. J., Saal, H. M., Zonana, J., Jones, M. C., Mascarello, J. T., and Emanuel, B. S. (1992b). Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome. Am. J. Hum. Genet. 44: 261-268.
-
(1992)
Am. J. Hum. Genet.
, vol.44
, pp. 261-268
-
-
Driscoll, D.A.1
Spinner, N.B.2
Budarf, M.L.3
McDonald-McGinn, D.M.4
Zackai, E.H.5
Goldberg, R.B.6
Shprintzen, R.J.7
Saal, H.M.8
Zonana, J.9
Jones, M.C.10
Mascarello, J.T.11
Emanuel, B.S.12
-
37
-
-
0025021391
-
Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter
-
37. Dumanski, J. P., Geurts van Kessel, A. D. H. M., Ruttledge, M., Wladis, A., Sugawa, N., Collins, V. P., and Nordenskjold, M. (1990). Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter. Hum. Genet. 84: 291-222.
-
(1990)
Hum. Genet.
, vol.84
, pp. 291-1222
-
-
Dumanski, J.P.1
Geurts Van Kessel, A.D.H.M.2
Ruttledge, M.3
Wladis, A.4
Sugawa, N.5
Collins, V.P.6
Nordenskjold, M.7
-
38
-
-
0025992756
-
A map of 22 loci on human chromosome 22
-
38. Dumanski, J. P., Carlbom, E., Collins, V. P., Nordenskjold, M., Emanuel, B. S., Budarf, M. L., McDermid, H. E., Wolff, R., O'Connell, P., White, R., Lalouel, J.-M., and Leppert, M. (1991). A map of 22 loci on human chromosome 22. Genomics 11: 709-719.
-
(1991)
Genomics
, vol.11
, pp. 709-719
-
-
Dumanski, J.P.1
Carlbom, E.2
Collins, V.P.3
Nordenskjold, M.4
Emanuel, B.S.5
Budarf, M.L.6
McDermid, H.E.7
Wolff, R.8
O'Connell, P.9
White, R.10
Lalouel, J.-M.11
Leppert, M.12
-
39
-
-
0026526313
-
Chromosomal assignment of 38 human brain expressed sequence tags (ESTs) by analyzing fluorescently labeled PCR products from hybrid cell panels
-
39. Durkin, A. S., Maglott, D. R., and Nierman, W. C. (1992). Chromosomal assignment of 38 human brain expressed sequence tags (ESTs) by analyzing fluorescently labeled PCR products from hybrid cell panels. Genomics 14: 808-810.
-
(1992)
Genomics
, vol.14
, pp. 808-810
-
-
Durkin, A.S.1
Maglott, D.R.2
Nierman, W.C.3
-
40
-
-
0026321397
-
Report of the committee on the genetic constitution of chromosome 22
-
40. Emanuel, B. S., Budarf, M. L., and Seizinger, B. R. (1991). Report of the committee on the genetic constitution of chromosome 22. Cytogenet. Cell Genet. 58: 827-852.
-
(1991)
Cytogenet. Cell Genet.
, vol.58
, pp. 827-852
-
-
Emanuel, B.S.1
Budarf, M.L.2
Seizinger, B.R.3
-
41
-
-
0027748771
-
Molecular and phenotypic analysis of the chromosome 22 microdeletion syndromes
-
C. J. Epstein, Ed. Wiley-Liss, New York
-
41. Emanuel, B. S., Driscoll, D., Goldmuntz, E., Baldwin, S., Biegel, J., Zackai, E. H., McDonald-McGinn, D., Sellinger, B., Gorman, N., Williams, S., and Budarf, M. L. (1993). Molecular and phenotypic analysis of the chromosome 22 microdeletion syndromes. In "Phenotypic Mapping of Down Syndrome and Other Aneuploid Conditions" (C. J. Epstein, Ed.), Vol. 384, pp. 207-224, Wiley-Liss, New York.
-
(1993)
Phenotypic Mapping of Down Syndrome and Other Aneuploid Conditions
, vol.384
, pp. 207-224
-
-
Emanuel, B.S.1
Driscoll, D.2
Goldmuntz, E.3
Baldwin, S.4
Biegel, J.5
Zackai, E.H.6
McDonald-McGinn, D.7
Sellinger, B.8
Gorman, N.9
Williams, S.10
Budarf, M.L.11
-
42
-
-
0005497063
-
Heterogeneity of chromosome 22 breakpoint in Ph-positive acute lymphocytic leukemia
-
42. Erikson, J., Griffin, C., ar-Rushdi, A., Valtieri, M., Hoxie, J., Finan, J., Emanuel, B. S., Rovera, G., Nowell, P. C., and Croce, C. M. (1986). Heterogeneity of chromosome 22 breakpoint in Ph-positive acute lymphocytic leukemia. Proc. Natl. Acad. Sci. USA 83: 1807-1811.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 1807-1811
-
-
Erikson, J.1
Griffin, C.2
Ar-Rushdi, A.3
Valtieri, M.4
Hoxie, J.5
Finan, J.6
Emanuel, B.S.7
Rovera, G.8
Nowell, P.C.9
Croce, C.M.10
-
43
-
-
0021381028
-
Addendum: A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
-
43. Feinberg, A. P., and Vogelstein, B. (1984). Addendum: A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem. 137: 266-267.
-
(1984)
Anal. Biochem.
, vol.137
, pp. 266-267
-
-
Feinberg, A.P.1
Vogelstein, B.2
-
44
-
-
0028798545
-
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
-
44. Flint, J., Wilkie, A. D., Buckle, V. J., Winter, R. M., Holland, A. J., and McDermid, H. E. (1995). The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nature Genet. 9: 312.
-
(1995)
Nature Genet.
, vol.9
, pp. 312
-
-
Flint, J.1
Wilkie, A.D.2
Buckle, V.J.3
Winter, R.M.4
Holland, A.J.5
McDermid, H.E.6
-
45
-
-
0003054793
-
Identification of a GTP-binding protein alpha subunit that lacks an apparent ADP-ribosylation site for pertussis toxin
-
45. Fong, H. K. W., Yoshimoto, K. K., Eversole-Cire, P., and Simon, M. I. (1988). Identification of a GTP-binding protein alpha subunit that lacks an apparent ADP-ribosylation site for pertussis toxin. Proc. Natl. Acad. Sci. USA 85: 3066-3070.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 3066-3070
-
-
Fong, H.K.W.1
Yoshimoto, K.K.2
Eversole-Cire, P.3
Simon, M.I.4
-
46
-
-
0025187418
-
hXBP-1 (human X-box binding protein) displays a BanI polymorphism on human chromosome 5
-
46. Fontaine, B., Hanson, M. P., Liou, H-C., Glimcher, L. H., Rouleau, G. A., and Gusella, J. F. (1990). hXBP-1 (human X-box binding protein) displays a BanI polymorphism on human chromosome 5. Nucleic Acids Res. 18: 5578.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 5578
-
-
Fontaine, B.1
Hanson, M.P.2
Liou, H.-C.3
Glimcher, L.H.4
Rouleau, G.A.5
Gusella, J.F.6
-
47
-
-
0026564360
-
A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus
-
47. Frazer, K. A., Boehnke, M., Budarf, M. L., Wolff, R. K., Emanuel, B. S., Myers, R. M., and Cox, D. R. (1992). A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus. Genomics 14: 574-584.
-
(1992)
Genomics
, vol.14
, pp. 574-584
-
-
Frazer, K.A.1
Boehnke, M.2
Budarf, M.L.3
Wolff, R.K.4
Emanuel, B.S.5
Myers, R.M.6
Cox, D.R.7
-
48
-
-
0024253674
-
Partial physical map of human chromosome 21
-
48. Gardiner, K., Watkins, P., Munke, M., Drabkin, H., Jones, C., and Patterson, D. (1988). Partial physical map of human chromosome 21. Somatic Cell Mol. Genet. 14: 623-638.
-
(1988)
Somatic Cell Mol. Genet.
, vol.14
, pp. 623-638
-
-
Gardiner, K.1
Watkins, P.2
Munke, M.3
Drabkin, H.4
Jones, C.5
Patterson, D.6
-
49
-
-
0018954369
-
Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22
-
49. Geurts van Kessel, A. H. M., Westerveld, A., de Groot, P. G., Meera Khan, P., and Hagemeijer, A. (1980). Regional localization of the genes coding for human ACO2, ARSA, and NAGA on chromosome 22. Cytogenet. Cell Genet. 28: 169-172.
-
(1980)
Cytogenet. Cell Genet.
, vol.28
, pp. 169-172
-
-
Geurts Van Kessel, A.H.M.1
Westerveld, A.2
De Groot, P.G.3
Meera Khan, P.4
Hagemeijer, A.5
-
50
-
-
0020957754
-
Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybrids
-
50. Geurts van Kessel, A. H. M., Tetteroo, P. A. T., von dem Borne, A. E. G. Kr., Hagemeijer, A., and Bootsma, D. (1983). Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybrids. Proc. Natl. Acad. Sci. USA 80: 3748-3752.
-
(1983)
Proc. Natl. Acad. Sci. USA
, vol.80
, pp. 3748-3752
-
-
Geurts Van Kessel, A.H.M.1
Tetteroo, P.A.T.2
Von Dem Borne, A.E.G.Kr.3
Hagemeijer, A.4
Bootsma, D.5
-
51
-
-
0025339377
-
Human interleukine 2 receptor b-chain gene: Chromosomal localization and identification of 5′ regulatory sequences
-
51. Gnarra, J. R., Otani, H., Wang, M. G., McBride, O. W., Sharon, M., and Leonard, W. J. (1990). Human interleukine 2 receptor b-chain gene: Chromosomal localization and identification of 5′ regulatory sequences. Proc. Natl. Acad. Sci. USA 87: 3440-3444.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 3440-3444
-
-
Gnarra, J.R.1
Otani, H.2
Wang, M.G.3
McBride, O.W.4
Sharon, M.5
Leonard, W.J.6
-
52
-
-
0027442395
-
Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects
-
52. Goldmuntz, E., Driscoll, D., Budarf, M. L., Zackai, E. H., McDonald-McGinn, D. M., Biegel, J. A., and Emanuel, B. S. (1993). Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects. J. Med. Genet. 30: 807-812.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 807-812
-
-
Goldmuntz, E.1
Driscoll, D.2
Budarf, M.L.3
Zackai, E.H.4
McDonald-McGinn, D.M.5
Biegel, J.A.6
Emanuel, B.S.7
-
53
-
-
0029985819
-
Cloning, genomic oration, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndromes minimal critical region
-
in press
-
53. Goldmuntz, E., Wang, Z., Roe, B. A., and Budarf, M. L. (1996). Cloning, genomic oration, and chromosomal localization of human citrate transport protein to the DiGeorge/velocardiofacial syndromes minimal critical region. Genomics, in press.
-
(1996)
Genomics
-
-
Goldmuntz, E.1
Wang, Z.2
Roe, B.A.3
Budarf, M.L.4
-
54
-
-
0023954396
-
Human debrisoquine 4-hydroxylase (P45011d1): cDNA and deduced amino acid sequence and assignment of the CYP2D locus to chromosome 22
-
54. Gonzalez, F. J., Vilbois, F., Hardwick, J. P., McBride, O. W., Nebert, D. W., Gelboin, H. V., and Meyer, U. A. (1988). Human debrisoquine 4-hydroxylase (P45011D1): cDNA and deduced amino acid sequence and assignment of the CYP2D locus to chromosome 22. Genomics 2: 174-179.
-
(1988)
Genomics
, vol.2
, pp. 174-179
-
-
Gonzalez, F.J.1
Vilbois, F.2
Hardwick, J.P.3
McBride, O.W.4
Nebert, D.W.5
Gelboin, H.V.6
Meyer, U.A.7
-
55
-
-
0028231090
-
The 1993-94 Généthon human genetic linkage map
-
55. Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. (1994). The 1993-94 Généthon human genetic linkage map. Nature Genet. 7: 246-335.
-
(1994)
Nature Genet.
, vol.7
, pp. 246-335
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
57
-
-
18144441664
-
An anonymouse single copy chromosome 22 clone, D22S10 (22cl-18) identifies an RFLP with Psti
-
57. Hofker, M. H., Breuning, M. H., Bakker, E., van Ommen, G. J. B., and Pearson, P. L. (1985). An anonymouse single copy chromosome 22 clone, D22S10 (22cl-18) identifies an RFLP with PstI. Nucleic Acids Res. 13: 7167.
-
(1985)
Nucleic Acids Res.
, vol.13
, pp. 7167
-
-
Hofker, M.H.1
Breuning, M.H.2
Bakker, E.3
Van Ommen, G.J.B.4
Pearson, P.L.5
-
58
-
-
0028960739
-
Structure of human gene encoding sterol regulatory element binding proteins-1 (SREBF1) and localization of SREBF1 and SREBF2 to chromosomes 17p11.2 and 22q13
-
58. Hua, Z., Wu, J., Goldstein, J. L., Brown, M. S., and Hobbs, H. H. (1995). Structure of human gene encoding sterol regulatory element binding proteins-1 (SREBF1) and localization of SREBF1 and SREBF2 to chromosomes 17p11.2 and 22q13. Genomics 25: 667-673.
-
(1995)
Genomics
, vol.25
, pp. 667-673
-
-
Hua, Z.1
Wu, J.2
Goldstein, J.L.3
Brown, M.S.4
Hobbs, H.H.5
-
59
-
-
0028603302
-
Isolation and regional mapping of 110 chromosome 22 STSs
-
59. Hudson, T. J., Colbert, A. M. E., Reeve, M. P., Bae, J. S., Lee, M. K., Nussbaum, R. L., Budarf, M. L., Emanel, B. S., and Foote, S. (1994). Isolation and regional mapping of 110 chromosome 22 STSs. Genomics 24: 558-592.
-
(1994)
Genomics
, vol.24
, pp. 558-592
-
-
Hudson, T.J.1
Colbert, A.M.E.2
Reeve, M.P.3
Bae, J.S.4
Lee, M.K.5
Nussbaum, R.L.6
Budarf, M.L.7
Emanel, B.S.8
Foote, S.9
-
60
-
-
0025729958
-
Direct assignment of the human bB2 and bB3 crystallin genes to 22q11.2 → q12: Markers for neurofibromatosis 2
-
60. Hulsebos, T. J. M., Bijlsma, E. K., Geurts van Kessel, A. H. M., Brakenhoff, R. H., and Westerveld, A. (1991). Direct assignment of the human bB2 and bB3 crystallin genes to 22q11.2 → q12: Markers for neurofibromatosis 2. Cytogenet. Cell Genet. 56: 171-175.
-
(1991)
Cytogenet. Cell Genet.
, vol.56
, pp. 171-175
-
-
Hulsebos, T.J.M.1
Bijlsma, E.K.2
Geurts Van Kessel, A.H.M.3
Brakenhoff, R.H.4
Westerveld, A.5
-
61
-
-
0028326668
-
Exon scanning for mutation of the NF2 gene in schwannomas
-
61. Jacoby, L. B., MacCollin, M., Louis, D. N., Mohney, T., Rubio, M-P., Pulaski, K., Trofatter, J. A., Kley, N., Seizinger, B., Ramesh, V., and Gusella, J. F. (1994). Exon scanning for mutation of the NF2 gene in schwannomas. Hum. Mol. Genet. 3: 413-419.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 413-419
-
-
Jacoby, L.B.1
MacCollin, M.2
Louis, D.N.3
Mohney, T.4
Rubio, M.-P.5
Pulaski, K.6
Trofatter, J.A.7
Kley, N.8
Seizinger, B.9
Ramesh, V.10
Gusella, J.F.11
-
62
-
-
0023132496
-
Gene mapping and medical genetics. Human chromosome 22
-
62. Kaplan, J-C., Aurias, A., Julier, C., Prieur, M., and Szajnert, M-F. (1987). Gene mapping and medical genetics. Human chromosome 22. J. Med. Genet. 24: 65-78.
-
(1987)
J. Med. Genet.
, vol.24
, pp. 65-78
-
-
Kaplan, J.-C.1
Aurias, A.2
Julier, C.3
Prieur, M.4
Szajnert, M.-F.5
-
63
-
-
0029102665
-
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
-
63. Karayiorgou, M., Morris, M. A., Morrow, B., Shprintzen, R. J., Goldberg, R., Borrow, J., Gos, A., Nestadt, G., Wolyniec, P. S., Lasseter, V. K., Eisen, H., Childs, B., Kazazian, H. H., Kucherlapati, R., Antonarakis, S. E., Pulver, A. E., and Housman, D. E. (1995). Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc. Natl. Acad. Sci. USA 92: 7612-7616.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 7612-7616
-
-
Karayiorgou, M.1
Morris, M.A.2
Morrow, B.3
Shprintzen, R.J.4
Goldberg, R.5
Borrow, J.6
Gos, A.7
Nestadt, G.8
Wolyniec, P.S.9
Lasseter, V.K.10
Eisen, H.11
Childs, B.12
Kazazian, H.H.13
Kucherlapati, R.14
Antonarakis, S.E.15
Pulver, A.E.16
Housman, D.E.17
-
64
-
-
0028812603
-
The organization of the human immunoglobudlin 1 gene locus
-
64. Kawasaki, K., Minoshima, S., Schooler, K., Kudoh, J., Asakawa, S., de Jong, P. J., and Shimizu, N. (1995). The organization of the human immunoglobudlin 1 gene locus. Genome Res. 5: 125-135.
-
(1995)
Genome Res.
, vol.5
, pp. 125-135
-
-
Kawasaki, K.1
Minoshima, S.2
Schooler, K.3
Kudoh, J.4
Asakawa, S.5
De Jong, P.J.6
Shimizu, N.7
-
65
-
-
0027459424
-
Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22
-
65. Kelley, D., Goldberg, R., Wilson, D., Lindsay, E., Carey, A., Goodship, J., Burn, J., Cross, I., Shprintzen, R. J., and Scambler, P. J. (1993). Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22. Am. J. Med. Genet. 45: 308-312.
-
(1993)
Am. J. Med. Genet.
, vol.45
, pp. 308-312
-
-
Kelley, D.1
Goldberg, R.2
Wilson, D.3
Lindsay, E.4
Carey, A.5
Goodship, J.6
Burn, J.7
Cross, I.8
Shprintzen, R.J.9
Scambler, P.J.10
-
66
-
-
0020026258
-
The association of the DiGeorge anomalad with partial monosomy of chromosome 22
-
66. Kelley, R. I., Zackai, E. H., Emanuel, B. S., Kistenmacher, M., Greenberg, F., and Punnett, H. H. (1982). The association of the DiGeorge anomalad with partial monosomy of chromosome 22. J. Pediatr. 101: 197-200.
-
(1982)
J. Pediatr.
, vol.101
, pp. 197-200
-
-
Kelley, R.I.1
Zackai, E.H.2
Emanuel, B.S.3
Kistenmacher, M.4
Greenberg, F.5
Punnett, H.H.6
-
67
-
-
0023887318
-
Isolation and mapping of a polymorphic DNA sequence (pEFZ31) on chromosome 22 (D22S32)
-
67. Krapcho, K., Nakamura, Y., Fujimoto, E., Eldridge, R., Leppert, M., O'Connell, P., Lathrop, G. M., Laloule, J. M., and White, R. (1988). Isolation and mapping of a polymorphic DNA sequence (pEFZ31) on chromosome 22 (D22S32). Nucleic Acids Res. 16: 5221.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 5221
-
-
Krapcho, K.1
Nakamura, Y.2
Fujimoto, E.3
Eldridge, R.4
Leppert, M.5
O'Connell, P.6
Lathrop, G.M.7
Laloule, J.M.8
White, R.9
-
68
-
-
0028293023
-
Chromosomal localization of the human heme oxygenase genes: Heme oxygenase-1 (HMOX1) maps to chromosome 22q12 and heme oxygenase-2 (HMOX2) maps to chromosome 16p13.1
-
68. Kutty, R. K., Kutty, G., Rodriguez, I. R., Chader, G. J., and Wiggert, B. (1994). Chromosomal localization of the human heme oxygenase genes: Heme oxygenase-1 (HMOX1) maps to chromosome 22q12 and heme oxygenase-2 (HMOX2) maps to chromosome 16p13.1. Genomics 20: 513-516.
-
(1994)
Genomics
, vol.20
, pp. 513-516
-
-
Kutty, R.K.1
Kutty, G.2
Rodriguez, I.R.3
Chader, G.J.4
Wiggert, B.5
-
69
-
-
0024546495
-
Precise localization of NF1 to 17q11.2 by balanced translocation
-
69. Ledbetter, D. H., Rich, D. C., O'Connell, P., Leppert, M., and Carey, J. C. (1989). Precise localization of NF1 to 17q11.2 by balanced translocation. Am. J. Hum. Genet. 44: 20-24.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 20-24
-
-
Ledbetter, D.H.1
Rich, D.C.2
O'Connell, P.3
Leppert, M.4
Carey, J.C.5
-
70
-
-
0024042469
-
The structure and organization of the human heavy neurofilament subunit (NF-H) and the gene encoding it
-
70. Lees, J. F., Shneidman, P. S., Skuntz, S. F., Garden, M. J., and Lazzarini, R. A. (1988). The structure and organization of the human heavy neurofilament subunit (NF-H) and the gene encoding it. EMBO J. 7: 1947-1955.
-
(1988)
EMBO J.
, vol.7
, pp. 1947-1955
-
-
Lees, J.F.1
Shneidman, P.S.2
Skuntz, S.F.3
Garden, M.J.4
Lazzarini, R.A.5
-
71
-
-
0025094268
-
Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines
-
71. Lichter, P., Ledbetter, S. A., Ledbetter, D. H., and Ward, D. C. (1990). Fluorescence in situ hybridization with Alu and L1 polymerase chain reaction probes for rapid characterization of human chromosomes in hybrid cell lines. Proc. Natl. Acad. Sci. USA 87: 6634-6638.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 6634-6638
-
-
Lichter, P.1
Ledbetter, S.A.2
Ledbetter, D.H.3
Ward, D.C.4
-
72
-
-
0028278792
-
Mapping of a human A2a adenosine receptor (ADORA2) to chromosome 22
-
72. MacCollin, M., Peterfreund, R., MacDonald, M., Fink, J. S., and Gusella, J. (1994). Mapping of a human A2a adenosine receptor (ADORA2) to chromosome 22. Genomics 20: 332-333.
-
(1994)
Genomics
, vol.20
, pp. 332-333
-
-
MacCollin, M.1
Peterfreund, R.2
MacDonald, M.3
Fink, J.S.4
Gusella, J.5
-
73
-
-
0027471649
-
A set of STS assays targeting the chromosome 22 physical framework markers
-
73. MacCollin, M., Romano, D., Budarf, M., Denny, C., Trofatter, J., Menon, A., Rouleau, G., Fontaine, B., Emanuel, B., and Gusella, J. (1993). A set of STS assays targeting the chromosome 22 physical framework markers. Genomics 15: 680-683.
-
(1993)
Genomics
, vol.15
, pp. 680-683
-
-
MacCollin, M.1
Romano, D.2
Budarf, M.3
Denny, C.4
Trofatter, J.5
Menon, A.6
Rouleau, G.7
Fontaine, B.8
Emanuel, B.9
Gusella, J.10
-
74
-
-
0027126644
-
Dinucleotide repeat polymorphism at the D22S264 locus
-
74. Marineau, C., Aubry, M., Julien, J. P., and Rouleau, G. A. (1991). Dinucleotide repeat polymorphism at the D22S264 locus. Nucleic Acids Res. 20: 1430.
-
(1991)
Nucleic Acids Res.
, vol.20
, pp. 1430
-
-
Marineau, C.1
Aubry, M.2
Julien, J.P.3
Rouleau, G.A.4
-
75
-
-
0027223234
-
Dinucleotide repeat polymorphism at the D22S268 locus
-
75. Marineau, C., Baron, C., Delattre, O., Zucman, J., Thomas, G., and Rouleau, G. A. (1993). Dinucleotide repeat polymorphism at the D22S268 locus. Hum. Mol. Genet. 2: 336.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 336
-
-
Marineau, C.1
Baron, C.2
Delattre, O.3
Zucman, J.4
Thomas, G.5
Rouleau, G.A.6
-
76
-
-
0022479573
-
Characterization of the supernumerary chromosome in Cat Eye syndrome
-
76. McDermid, H. E., Duncan, A. M. V., Brasch, K. R., Holden, J. J. A., Magenis, E., Sheehy, R., Burn, J., Kardon, N., Noel, B., Schinzel, A., Teshima, I., and White, B. N. (1986). Characterization of the supernumerary chromosome in Cat Eye syndrome. Science 232: 646-648.
-
(1986)
Science
, vol.232
, pp. 646-648
-
-
McDermid, H.E.1
Duncan, A.M.V.2
Brasch, K.R.3
Holden, J.J.A.4
Magenis, E.5
Sheehy, R.6
Burn, J.7
Kardon, N.8
Noel, B.9
Schinzel, A.10
Teshima, I.11
White, B.N.12
-
77
-
-
0024694163
-
Toward a long-range map of human chromosomal band 22q11
-
77. McDermid, H. E., Budarf, M. L., and Emanuel, B. S. (1989). Toward a long-range map of human chromosomal band 22q11. Genomics 5: 1-8.
-
(1989)
Genomics
, vol.5
, pp. 1-8
-
-
McDermid, H.E.1
Budarf, M.L.2
Emanuel, B.S.3
-
78
-
-
0027521344
-
Long-range restriction map of 22q11-22q12 between the lambda immunoglobulin locus and the Ewings sarcoma breakpoint
-
78. McDermid, H. E., Budarf, M. L., and Emanuel, B. E. (1993). Long-range restriction map of 22q11-22q12 between the lambda immunoglobulin locus and the Ewings sarcoma breakpoint. Genomics 18: 308-318.
-
(1993)
Genomics
, vol.18
, pp. 308-318
-
-
McDermid, H.E.1
Budarf, M.L.2
Emanuel, B.E.3
-
79
-
-
0029148704
-
Autosomal dominant Opitz syndrome due to a 22q11.2 deletion
-
79. McDonald-McGinn, D. M., Driscoll, D. A., Bason, L., Christensen, K., Lynch, D., Sullivan, K., Canning, D., Zavod, W., Quinn, N., Weinberg, P., Clark, B. J., Emanuel, B. S., and Zackai, E. H. (1995). Autosomal dominant Opitz syndrome due to a 22q11.2 deletion. Am. J. Med. Genet. 59: 103-113.
-
(1995)
Am. J. Med. Genet.
, vol.59
, pp. 103-113
-
-
McDonald-McGinn, D.M.1
Driscoll, D.A.2
Bason, L.3
Christensen, K.4
Lynch, D.5
Sullivan, K.6
Canning, D.7
Zavod, W.8
Quinn, N.9
Weinberg, P.10
Clark, B.J.11
Emanuel, B.S.12
Zackai, E.H.13
-
80
-
-
0027535454
-
Two members of the S-lac lectin gene family, LGALS1 and LGALS2, reside in close proximity on human chromosome 22q12-q13
-
80. Mehrabian, M., Gitt, M. A., Sparkes, R. S., Leffler, H., Barondes, S. H., and Lusis, A. J. (1993). Two members of the S-lac lectin gene family, LGALS1 and LGALS2, reside in close proximity on human chromosome 22q12-q13. Genomics 15: 418-420.
-
(1993)
Genomics
, vol.15
, pp. 418-420
-
-
Mehrabian, M.1
Gitt, M.A.2
Sparkes, R.S.3
Leffler, H.4
Barondes, S.H.5
Lusis, A.J.6
-
81
-
-
0025901088
-
Parameters of the human genome
-
81. Morton, N. E. (1991). Parameters of the human genome. Proc. Natl. Acad. Sci. USA 88: 7474-7476.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 7474-7476
-
-
Morton, N.E.1
-
82
-
-
0021414573
-
DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22
-
82. Naylor, S. L., Sakaguchi, A. Y., Barker, D., White, R., and Shows, T. B. (1984). DNA polymorphic loci mapped to human chromosomes 3, 5, 9, 11, 17, 18, and 22. Proc. Natl. Acad. Sci. USA 81: 2447-2451.
-
(1984)
Proc. Natl. Acad. Sci. USA
, vol.81
, pp. 2447-2451
-
-
Naylor, S.L.1
Sakaguchi, A.Y.2
Barker, D.3
White, R.4
Shows, T.B.5
-
83
-
-
0025254309
-
An alternatively processed mRNA specific for g-glutamyl transpeptidase in human tissues
-
83. Pawlak, A., Cohen, E. H., Octave, J-N., Schweickhardt, R., Wu, S-J., Bulle, F., Chikhi, N., Baik, J-H., Siegrist, S., and Guellaen, G. (1990). An alternatively processed mRNA specific for g-glutamyl transpeptidase in human tissues. J. Biol. Chem. 265: 3256-3262.
-
(1990)
J. Biol. Chem.
, vol.265
, pp. 3256-3262
-
-
Pawlak, A.1
Cohen, E.H.2
Octave, J.-N.3
Schweickhardt, R.4
Wu, S.-J.5
Bulle, F.6
Chikhi, N.7
Baik, J.-H.8
Siegrist, S.9
Guellaen, G.10
-
84
-
-
0025880644
-
The cDNA sequence and the deduced amino acid sequence of human transcobalamin II show homology with rat intrinsic factor and human transcobalamin I
-
84. Platica, O., Janecko, R., Quadros, E. V., Regec, A., Romain, R., and Rothenberg, S. P. (1991). The cDNA sequence and the deduced amino acid sequence of human transcobalamin II show homology with rat intrinsic factor and human transcobalamin I. J. Biol. Chem. 256: 7860-7863.
-
(1991)
J. Biol. Chem.
, vol.256
, pp. 7860-7863
-
-
Platica, O.1
Janecko, R.2
Quadros, E.V.3
Regec, A.4
Romain, R.5
Rothenberg, S.P.6
-
85
-
-
0025131060
-
A BamHI RFLP in the human arylsulfatase A gene
-
85. Polten, A., and Gieselmann, V. (1990). A BamHI RFLP in the human arylsulfatase A gene. Nucleic Acids Res. 18: 6746.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 6746
-
-
Polten, A.1
Gieselmann, V.2
-
86
-
-
0026579547
-
Chromosomal assignment of 46 brain cDNAs
-
86. Polymeropoulos, M., Xiao, H., Glodek, A., Gorski, M., Adams, M. D., Moreno, R. F., Fitzgerald, M. G., Venter, J. C., and Merril, C. R. (1992). Chromosomal assignment of 46 brain cDNAs. Genomics 12: 492-496.
-
(1992)
Genomics
, vol.12
, pp. 492-496
-
-
Polymeropoulos, M.1
Xiao, H.2
Glodek, A.3
Gorski, M.4
Adams, M.D.5
Moreno, R.F.6
Fitzgerald, M.G.7
Venter, J.C.8
Merril, C.R.9
-
87
-
-
0027268587
-
Chromosomal distribution of 320 genes from a brain cDNA library
-
87. Polymeropoulos, M. H., Xiao, H., Sikela, J. M., Adams, M., Venter, J. C., and Merrill, C. R. (1993). Chromosomal distribution of 320 genes from a brain cDNA library. Nature Genet. 4: 381-386.
-
(1993)
Nature Genet.
, vol.4
, pp. 381-386
-
-
Polymeropoulos, M.H.1
Xiao, H.2
Sikela, J.M.3
Adams, M.4
Venter, J.C.5
Merrill, C.R.6
-
88
-
-
0027447683
-
Twelve new polymorphic microsatellites on human chromosome 22
-
88. Porter, J. C., Ram, K. T., and Puck, J. M. (1993). Twelve new polymorphic microsatellites on human chromosome 22. Genomics 15: 57-61.
-
(1993)
Genomics
, vol.15
, pp. 57-61
-
-
Porter, J.C.1
Ram, K.T.2
Puck, J.M.3
-
89
-
-
23444436161
-
Seven chromosome 22 STR polymorphisms
-
89. Porter, J. C., and Puck, J. M. (1994). Seven chromosome 22 STR polymorphisms. Hum. Mol. Genet. 3: 519.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 519
-
-
Porter, J.C.1
Puck, J.M.2
-
90
-
-
0024524581
-
Molecular cloning of cDNA encoding the p70 (Ku) lupus autoantigen
-
90. Reeves, W. H., and Sthoeger, Z. M. (1989). Molecular cloning of cDNA encoding the p70 (Ku) lupus autoantigen. J. Biol. Chem. 264: 5047-5052.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 5047-5052
-
-
Reeves, W.H.1
Sthoeger, Z.M.2
-
91
-
-
0028881136
-
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2
-
91. Robin, N. H., Feldman, G. J., Aronson, A. L., Mitchell, M. F., Weksberg, R., Leonard, C. O., Burton, B. K., Josephson, K. D., Laxova, R., Aleck, K. A., Allanson, J. E., Guion-almeida, M. L., Martin, R. A., Leichtman, L. G., Price, R. A., Opitz, J. M., and Muenke, M. (1995). Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2. Nature Genet. 11: 459-461.
-
(1995)
Nature Genet.
, vol.11
, pp. 459-461
-
-
Robin, N.H.1
Feldman, G.J.2
Aronson, A.L.3
Mitchell, M.F.4
Weksberg, R.5
Leonard, C.O.6
Burton, B.K.7
Josephson, K.D.8
Laxova, R.9
Aleck, K.A.10
Allanson, J.E.11
Guion-Almeida, M.L.12
Martin, R.A.13
Leichtman, L.G.14
Price, R.A.15
Opitz, J.M.16
Muenke, M.17
-
92
-
-
0026051784
-
Oncostatin M is a member of a cytokine family that includes leukemia-inhibitory factor, granulocyte colony-stimulating factor, and interleukin 6
-
92. Rose, T. M., and Bruce, G. (1991). Oncostatin M is a member of a cytokine family that includes leukemia-inhibitory factor, granulocyte colony-stimulating factor, and interleukin 6. Proc. Natl. Acad. Sci. USA 88: 8641-8645.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 8641-8645
-
-
Rose, T.M.1
Bruce, G.2
-
93
-
-
0024567429
-
A genetic linkage map of the long arm of human chromosome 22
-
93. Rouleau, G. A., Haines, J. L., Bazanowski, A., Colella-Crowley, A., Trofatter, J. A., Wexler, N. S., Conneally, P. M., and Gusella, J. F. (1989). A genetic linkage map of the long arm of human chromosome 22. Genomics 4: 1-6.
-
(1989)
Genomics
, vol.4
, pp. 1-6
-
-
Rouleau, G.A.1
Haines, J.L.2
Bazanowski, A.3
Colella-Crowley, A.4
Trofatter, J.A.5
Wexler, N.S.6
Conneally, P.M.7
Gusella, J.F.8
-
94
-
-
0028055068
-
Physical mapping of the NF2/ meningioma region on human chromosome 22q12
-
94. Ruttledge, M. H., Xie, Y-G., Han, F-Y., Giovannini, M., Janson, M., Fransson, I., Werelius, B., Delattre, O., Thomas, G., Evans, G., and Dumanski, J. P. (1994a). Physical mapping of the NF2/ meningioma region on human chromosome 22q12. Genomics 19: 52-59.
-
(1994)
Genomics
, vol.19
, pp. 52-59
-
-
Ruttledge, M.H.1
Xie, Y.-G.2
Han, F.-Y.3
Giovannini, M.4
Janson, M.5
Fransson, I.6
Werelius, B.7
Delattre, O.8
Thomas, G.9
Evans, G.10
Dumanski, J.P.11
-
95
-
-
0028276445
-
Deletions in chromosome 22 in sporadic meningioma
-
95. Ruttledge, M. H., Xie, Y-G., Han, F-Y., Peyrard, M., Collins, V. P., Nordenskjold, M., and Dumanski, J. P. (1994b). Deletions in chromosome 22 in sporadic meningioma. Genes Chromosomes Cancer 10: 122-130.
-
(1994)
Genes Chromosomes Cancer
, vol.10
, pp. 122-130
-
-
Ruttledge, M.H.1
Xie, Y.-G.2
Han, F.-Y.3
Peyrard, M.4
Collins, V.P.5
Nordenskjold, M.6
Dumanski, J.P.7
-
96
-
-
0025174075
-
Human nonmuscle myosin heavy chain mRNA: Generation of diversity through alternative polyadenylylation
-
96. Saez, C. G., Myers, J. C., Shows, T. B., and Leinwand, L. A. (1990). Human nonmuscle myosin heavy chain mRNA: Generation of diversity through alternative polyadenylylation. Proc. Natl. Acad. Sci. USA 87: 1164-1168.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 1164-1168
-
-
Saez, C.G.1
Myers, J.C.2
Shows, T.B.3
Leinwand, L.A.4
-
97
-
-
0023237159
-
Gene deletions correlate with the development of alloantibodies in von Willebrand disease
-
97. Shelton-Inloes, B. B., Chehab, F. F., Mannucci, P. M., Federici, A. B., and Sadler, J. E. (1987). Gene deletions correlate with the development of alloantibodies in von Willebrand disease. J. Clin. Invest. 79: 1459-1465.
-
(1987)
J. Clin. Invest.
, vol.79
, pp. 1459-1465
-
-
Shelton-Inloes, B.B.1
Chehab, F.F.2
Mannucci, P.M.3
Federici, A.B.4
Sadler, J.E.5
-
98
-
-
0021802841
-
Fused transcript of abl and bcr genes in chronic myelogenous leukemia
-
98. Shtivelman, E., Lifshitz, B., Gale, R., and Canaani, E. (1985). Fused transcript of abl and bcr genes in chronic myelogenous leukemia. Nature (London) 315: 550-554.
-
(1985)
Nature (London)
, vol.315
, pp. 550-554
-
-
Shtivelman, E.1
Lifshitz, B.2
Gale, R.3
Canaani, E.4
-
99
-
-
0026849420
-
A mutation in adenylosuccinate lyase associated with mental retardation and autistic features
-
99. Stone, R. L., Aimi, J., Barshop, B. A., Jaeken, J., Van den Berghe, G., Zalkin, H., and Dixon, J. E. (1992). A mutation in adenylosuccinate lyase associated with mental retardation and autistic features. Nature Genet. 1: 59.
-
(1992)
Nature Genet.
, vol.1
, pp. 59
-
-
Stone, R.L.1
Aimi, J.2
Barshop, B.A.3
Jaeken, J.4
Van Den Berghe, G.5
Zalkin, H.6
Dixon, J.E.7
-
100
-
-
0022423487
-
Cloning and sequencing of a rearranged V1 gene from a Burkitt's lymphoma cell line expressing kappa light chains
-
100. Sun, L.-H. K., Croce, C. M., and Showe, L. C. (1985). Cloning and sequencing of a rearranged V1 gene from a Burkitt's lymphoma cell line expressing kappa light chains. Nucleic Acids Res. 13: 4921-4934.
-
(1985)
Nucleic Acids Res.
, vol.13
, pp. 4921-4934
-
-
Sun, L.-H.K.1
Croce, C.M.2
Showe, L.C.3
-
101
-
-
0028904495
-
Molecular cloning of a cDNA and chromosomal localization of a human theta-class glutathione S-transferase gene (GSTT2) to chromosome
-
101. Tan, K. L., Webb, G. C., Baker, R. T., and Board, P. G. (1995). Molecular cloning of a cDNA and chromosomal localization of a human theta-class glutathione S-transferase gene (GSTT2) to chromosome. Genomics 25: 381-387.
-
(1995)
Genomics
, vol.25
, pp. 381-387
-
-
Tan, K.L.1
Webb, G.C.2
Baker, R.T.3
Board, P.G.4
-
102
-
-
0026918945
-
Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2)
-
102. Trofatter, J. A., Systma, M. L., Gusella, J. F., and Haines, J. L. (1992). Dinucleotide repeat polymorphism at the topoisomerase (DNA) I pseudogene 2 (TOPIP2). Hum. Mol. Genet. 1: 455.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 455
-
-
Trofatter, J.A.1
Systma, M.L.2
Gusella, J.F.3
Haines, J.L.4
-
103
-
-
0021771487
-
Molecular cloning of human immunoglobulin 1 chain variable sequence
-
103. Tsuijimoto, Y., and Croce, C. M. (1984). Molecular cloning of human immunoglobulin 1 chain variable sequence. Nucleic Acids Res. 12: 8407-8414.
-
(1984)
Nucleic Acids Res.
, vol.12
, pp. 8407-8414
-
-
Tsuijimoto, Y.1
Croce, C.M.2
-
104
-
-
0028363004
-
Genetic mapping of 14 short tandem repeat polymorphisms on human chromosome 22
-
104. Vallada, H. P., Collins, J. E., Dunham, I., Dawson, E., Murray, R. M., Gill, M., and Collier, D. A. (1994). Genetic mapping of 14 short tandem repeat polymorphisms on human chromosome 22. Hum. Genet. 93: 688-690.
-
(1994)
Hum. Genet.
, vol.93
, pp. 688-690
-
-
Vallada, H.P.1
Collins, J.E.2
Dunham, I.3
Dawson, E.4
Murray, R.M.5
Gill, M.6
Collier, D.A.7
-
105
-
-
0027532176
-
Isolation and characterization of 25 unique DNA markers for human chromosome 22
-
105. Van Biezen, N. A., Lekanne Deprez, R. H., Thijs, A., Heutink, P., Oostra, B. A., Geurts van Kessel, A. D. H., and Zwarthoff, E. C. (1993). Isolation and characterization of 25 unique DNA markers for human chromosome 22. Genomics 15: 206-208.
-
(1993)
Genomics
, vol.15
, pp. 206-208
-
-
Van Biezen, N.A.1
Lekanne Deprez, R.H.2
Thijs, A.3
Heutink, P.4
Oostra, B.A.5
Geurts Van Kessel, A.D.H.6
Zwarthoff, E.C.7
-
106
-
-
0023240014
-
A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity
-
106. van Keuren, M. L., Hart, I. M., Kao, F.-T., Neve, R. L., Bruns, G. A. P., Kurnit, D. M., and Patterson, D. (1987). A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity. Cytogenet. Cell Genet. 44: 142-147.
-
(1987)
Cytogenet. Cell Genet.
, vol.44
, pp. 142-147
-
-
Van Keuren, M.L.1
Hart, I.M.2
Kao, F.-T.3
Neve, R.L.4
Bruns, G.A.P.5
Kurnit, D.M.6
Patterson, D.7
-
107
-
-
0025705607
-
Dinucleotides repeat polymorphism at the D22S156 locus
-
107. Weber, J. L. (1990). Dinucleotides repeat polymorphism at the D22S156 locus. Nucleic Acid Res. 18: 4639.
-
(1990)
Nucleic Acid Res.
, vol.18
, pp. 4639
-
-
Weber, J.L.1
-
108
-
-
0026446099
-
A second-generation linkage map of the human genome
-
108. Weissenbach, J., Gyapay, G., Dib, C., Vignal, A., Morissette, J., Millasseau, P., Vaysseix, G., and Lathrop, M. (1992). A second-generation linkage map of the human genome. Nature 359: 794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
109
-
-
0021380384
-
Organization of the human myoglobin gene
-
109. Weller, P., Jeffreys, J. A., Wilson, V., and Blanchetot, A. (1984). Organization of the human myoglobin gene. EMBO J. 3: 439-446.
-
(1984)
EMBO J.
, vol.3
, pp. 439-446
-
-
Weller, P.1
Jeffreys, J.A.2
Wilson, V.3
Blanchetot, A.4
-
110
-
-
0026725876
-
Deletions within chromosome 22q11 in familial congenital heart disease
-
110. Wilson, D. I., Goodship, J. A., Burn, J., Cross, I. E., and Scambler, P. J. (1992). Deletions within chromosome 22q11 in familial congenital heart disease. Lancet 340: 573-575.
-
(1992)
Lancet
, vol.340
, pp. 573-575
-
-
Wilson, D.I.1
Goodship, J.A.2
Burn, J.3
Cross, I.E.4
Scambler, P.J.5
-
111
-
-
0027460373
-
Human somatostatin receptor genes: Localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms
-
111. Yamada, Y., Stoffel, M., Espinosa, R., Xiang, K. S., Seino, M., Seino, S., Le Beau, M. M., and Bell, G. I. (1993). Human somatostatin receptor genes: Localization to human chromosomes 14, 17, and 22 and identification of simple tandem repeat polymorphisms. Genomics 15: 449-452.
-
(1993)
Genomics
, vol.15
, pp. 449-452
-
-
Yamada, Y.1
Stoffel, M.2
Espinosa, R.3
Xiang, K.S.4
Seino, M.5
Seino, S.6
Le Beau, M.M.7
Bell, G.I.8
|