-
1
-
-
0023800151
-
Trisomy 18: A nine year review
-
Bergin, A., McManus, S. P., Clarke, T. A., and Moloney, M. (1988). Trisomy 18: A nine year review. Ir. J. Med. Sci. 157: 5-7.
-
(1988)
Ir. J. Med. Sci
, vol.157
, pp. 5-7
-
-
Bergin, A.1
McManus, S.P.2
Clarke, T.A.3
Moloney, M.4
-
2
-
-
0026716244
-
A molecular defect in human protoporphyria
-
Brenner, D. A., Didier, J. M., Frasier, F., Cristensen, S. R., Evans, G. A., and Dailey, H. A. (1992). A molecular defect in human protoporphyria. Am. J. Hum. Genet. 50: 1203-1210.
-
(1992)
Am. J. Hum. Genet
, vol.50
, pp. 1203-1210
-
-
Brenner, D.A.1
Didier, J.M.2
Frasier, F.3
Cristensen, S.R.4
Evans, G.A.5
Dailey, H.A.6
-
3
-
-
0025942732
-
Influence of aberrant observations on high-resolution linkage analysis outcomes
-
Buetow, K. H. (1991). Influence of aberrant observations on high-resolution linkage analysis outcomes. Am. J. Hum. Genet. 49: 985-994.
-
(1991)
Am. J. Hum. Genet
, vol.49
, pp. 985-994
-
-
Buetow, K.H.1
-
4
-
-
0022194309
-
Report of the committee on methods of linkage analysis and reporting
-
Conneally, P. M., Edwards, J. H., Kidd, K. K., Lalouel, J. M., Morton, N. E., Ott, J., and White, R. (1985). Report of the committee on methods of linkage analysis and reporting. Cytogenet. Cell Genet. 40: 356-359.
-
(1985)
Cytogenet. Cell Genet
, vol.40
, pp. 356-359
-
-
Conneally, P.M.1
Edwards, J.H.2
Kidd, K.K.3
Lalouel, J.M.4
Morton, N.E.5
Ott, J.6
White, R.7
-
5
-
-
0023663060
-
A genetic linkage map of the human genome
-
Donis-Keller, H., Green, P., Helms, C., Cartinhour, S., Weiffenbach, B., Stephens, K., Keith, T. P., Bowden, D. W., Smith, D. R., Lander, E. S., Botstein, D., Akots, G., Rediker, K. S., Gravius, T., Brown, V. A., Rising, M. B., Parker, C., Powers, J. A., Watt, D. E., Kauffman, E. R., Bricker, A., Phipps, P., Muller-Kahle, H., Fulton, T. R., Ng, S., Schumm, J. W., Braman, J. C., Knowlton, R. G., Barker, D. F., Crooks, S. M., Lincoln, S. E., Daly, M. J., and Abrahamson, J. (1987). A genetic linkage map of the human genome. Cell 51: 319-337.
-
(1987)
Cell
, vol.51
, pp. 319-337
-
-
Donis-Keller, H.1
Green, P.2
Helms, C.3
Cartinhour, S.4
Weiffenbach, B.5
Stephens, K.6
Keith, T.P.7
Bowden, D.W.8
Smith, D.R.9
Lander, E.S.10
Botstein, D.11
Akots, G.12
Rediker, K.S.13
Gravius, T.14
Brown, V.A.15
Rising, M.B.16
Parker, C.17
Powers, J.A.18
Watt, D.E.19
Kauffman, E.R.20
Bricker, A.21
Phipps, P.22
Muller-Kahle, H.23
Fulton, T.R.24
Ng, S.25
Schumm, J.W.26
Braman, J.C.27
Knowlton, R.G.28
Barker, D.F.29
Crooks, S.M.30
Lincoln, S.E.31
Daly, M.J.32
Abrahamson, J.33
more..
-
6
-
-
85027641242
-
(1991). Mutations of transthyretin (TTR) gene in Italy
-
Ferlini, A., Saraiva, M. J., Almeida, M. R., Salvi, F., Plasmati, R., Tassinari, C. A., Costa, P. P., and Forabosco, A. (1991). Mutations of transthyretin (TTR) gene in Italy. Cytogenet. Cell Genet. 58: 2013.
-
(2013)
Cytogenet. Cell Genet
, pp. 58
-
-
Ferlini, A.1
Saraiva, M.J.2
Almeida, M.R.3
Salvi, F.4
Plasmati, R.5
Tassinari, C.A.6
Costa, P.P.7
Forabosco, A.8
-
7
-
-
0024284368
-
Isolation and mapping of a polymorphic DNA sequence (PHHHl63) on chromosome 18
-
Hoff, M., Nakamura, Y., O'Connell, P., Leppert, M., Lathrop, G. M., Laiouel, J. M., and White, R. (1988). Isolation and mapping of a polymorphic DNA sequence (pHHHl63) on chromosome 18. Nucleic Acids. Res. 16: 4189.
-
(1988)
Nucleic Acids. Res
, vol.16
, pp. 4189
-
-
Hoff, M.1
Nakamura, Y.2
O'connell, P.3
Leppert, M.4
Lathrop, G.M.5
Laiouel, J.M.6
White, R.7
-
8
-
-
0026653164
-
Frequent loss of expression of the potential tumor supressor gene DCC in ductal pancreatic adenocarcinoma
-
Hohne, M. W., Halatsch, M. E., Kahl, G. F., and Weinel, R. J. (1992). Frequent loss of expression of the potential tumor supressor gene DCC in ductal pancreatic adenocarcinoma. Cancer Res. 52: 2616-2619.
-
(1992)
Cancer Res
, vol.52
, pp. 2616-2619
-
-
Hohne, M.W.1
Halatsch, M.E.2
Kahl, G.F.3
Weinel, R.J.4
-
9
-
-
0026736249
-
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms
-
Hudson, T. J., Engelstein, M., Lee, M. K., Ho, E. C., Rubenfield, M. J., Adams, C. P., Housman, D. E., and Dracopoli, N. C. (1992). Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics 13: 622-629.
-
(1992)
Genomics
, vol.13
, pp. 622-629
-
-
Hudson, T.J.1
Engelstein, M.2
Lee, M.K.3
Ho, E.C.4
Rubenfield, M.J.5
Adams, C.P.6
Housman, D.E.7
Dracopoli, N.C.8
-
10
-
-
0026132133
-
(
-
Keats, B. J. B., Sherman, S. L., Morton, N. E., Robson, E. B., Buetow, K. H., Cartwright, P. E., Chakravarti, A., Francke, U, Green, P. P., and Ott, J. (1991). Guidelines for human linkage maps: An international system for human linkage maps. Genomics 9: 557-560.
-
(1991)
Genomics
, vol.9
, pp. 557-560
-
-
Keats, B.J.B.1
Sherman, S.L.2
Morton, N.E.3
Robson, E.B.4
Buetow, K.H.5
Cartwright, P.E.6
Chakravarti, A.7
Francke, U.8
Green, P.P.9
Ott, J.10
-
11
-
-
0026588314
-
Somatic cell hybrid deletion map of human chromosome 18
-
Kline, A. D., Rojas, K., Mewar, R., Moshinsky, D., and Overhauser, J. (1992). Somatic cell hybrid deletion map of human chromosome 18, Genomics 13: 1-6.
-
(1992)
Genomics
, vol.13
, pp. 1-6
-
-
Kline, A.D.1
Rojas, K.2
Mewar, R.3
Moshinsky, D.4
Overhauser, J.5
-
13
-
-
0022546835
-
Use of highly polymorphic DNA probes for genotypic analysis following bone marrow transplant
-
Knowlton, R. G., Brown, V. A., Braman, J. C., Barker, D., Schumm, J. W., Murray, C., Takvorian, T., Ritz, J., and Donis-Keller, H. (1986). Use of highly polymorphic DNA probes for genotypic analysis following bone marrow transplant. Blood 68: 378-385.
-
(1986)
Blood
, vol.68
, pp. 378-385
-
-
Knowlton, R.G.1
Brown, V.A.2
Braman, J.C.3
Barker, D.4
Schumm, J.W.5
Murray, C.6
Takvorian, T.7
Ritz, J.8
Donis-Keller, H.9
-
14
-
-
0024284002
-
Isolation of mapping of a polymorphic DNA sequence pEFZIO on chromosome 18
-
Krapcho, K., Nakamura, Y., Fujimoto, E., Ballard, L., O'Connell, P., Leppert, M., Lathrop, G. M., Laiouel, J. M., and White, R. (1988). Isolation of mapping of a polymorphic DNA sequence pEFZIO on chromosome 18. Nucleic Acids. Res. 16: 1227.
-
(1988)
Nucleic Acids. Res
, vol.16
, pp. 1227
-
-
Krapcho, K.1
Nakamura, Y.2
Fujimoto, E.3
Ballard, L.4
O'connell, P.5
Leppert, M.6
Lathrop, G.M.7
Laiouel, J.M.8
White, R.9
-
15
-
-
0026742086
-
Monosomy 18ql2.1 - 21.1: A recognizable aneuploidy syndrome? Report of a patient and review of the literature
-
Krasikov, N., Thompson, K., and Singh Sekhon, G. (1992). Monosomy 18ql2.1 - 21.1: A recognizable aneuploidy syndrome? Report of a patient and review of the literature. Am. J. Med. Genet. 43: 531-534.
-
(1992)
Am. J. Med. Genet
, vol.43
, pp. 531-534
-
-
Krasikov, N.1
Thompson, K.2
Singh Sekhon, G.3
-
16
-
-
0026582962
-
Construction of a GT polymorphism map of human 9q
-
Kwiatkowski, D. J., Henske, E. P., Weimer, K., Ozelius, L., Gusella, J. F., and Haines, J. (1992). Construction of a GT polymorphism map of human 9q. Genomics 12: 229-240.
-
(1992)
Genomics
, vol.12
, pp. 229-240
-
-
Kwiatkowski, D.J.1
Henske, E.P.2
Weimer, K.3
Ozelius, L.4
Gusella, J.F.5
Haines, J.6
-
17
-
-
0000803318
-
Construction of multilocus genetic linkage maps in humans
-
Lander, E. S., and Green, P. (1987). Construction of multilocus genetic linkage maps in humans. Proc. Natl. Acad. Sci. USA 84: 2363-2367.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 2363-2367
-
-
Lander, E.S.1
Green, P.2
-
18
-
-
0342499587
-
Strategies for multilocus linkage analysis in humans
-
Lathrop, G. M., Laiouel, J. M., Julier, C., and Ott, J. (1984). Strategies for multilocus linkage analysis in humans. Proc. Natl. Acad. Sci. USA 81: 3443-3446.
-
(1984)
Proc. Natl. Acad. Sci. USA
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Laiouel, J.M.2
Julier, C.3
Ott, J.4
-
19
-
-
0022646961
-
Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis
-
Lathrop, G. M., Laiouel, J. M., and White, R. L. (1986). Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis. Genet. Epidemiol. 3: 39-52.
-
(1986)
Genet. Epidemiol
, vol.3
, pp. 39-52
-
-
Lathrop, G.M.1
Laiouel, J.M.2
White, R.L.3
-
20
-
-
0026340022
-
Report of the committee on the genetic constitution of chromosome 18
-
Le Beau, M. M., and Geurts van Kessel, A H. M. (1991). Report of the committee on the genetic constitution of chromosome 18. Cytogenet. Cell Genet. 58: 739-750.
-
(1991)
Cytogenet. Cell Genet
, vol.58
, pp. 739-750
-
-
Le Beau, M.M.1
Geurts Van Kessel, A.2
-
21
-
-
85027646424
-
(1991). A somatic cell hybrid panel for regional mapping on human chromosome 1&. Cytogenet
-
Markie, D., Jones, T. A., Sheer, D., and Bodmer, W. F. (1991). A somatic cell hybrid panel for regional mapping on human chromosome 1&. Cytogenet. Cell Genet. 58: 2014. (Abstract)
-
Cell Genet
, vol.58
, pp. 2014
-
-
Markie, D.1
Jones, T.A.2
Sheer, D.3
Bodmer, W.F.4
-
22
-
-
0025901088
-
Parameters of the human genome. Proc
-
Morton, N. E. (1991). Parameters of the human genome. Proc. Natl. Acad. Sci. USA 88: 7474-7476.
-
(1991)
Natl. Acad. Sci. USA
, vol.88
, pp. 7474-7476
-
-
Morton, N.E.1
-
23
-
-
0023278777
-
Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18
-
Muller, U., Donlon, T. A., Harris, P., Rose, E., Hoffman, E., Bruns, G. P., and Latt, S. A. (1987). Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18. Cyto-, genet. Cell Genet. 45: 16-20.
-
(1987)
Cyto-, Genet. Cell Genet
, vol.45
, pp. 16-20
-
-
Muller, U.1
Donlon, T.A.2
Harris, P.3
Rose, E.4
Hoffman, E.5
Bruns, G.P.6
Latt, S.A.7
-
24
-
-
0024120348
-
Twelve loci form a continuous linkage map for human chromosome 18
-
O'Connell, P., Lathrop, G. M., Leppert, M., Nakamura, Y., Muller, U., Laiouel, J.-M., and White, R. (1988). Twelve loci form a continuous linkage map for human chromosome 18. Genomics 3: 367-372.
-
(1988)
Genomics
, vol.3
, pp. 367-372
-
-
O'connell, P.1
Lathrop, G.M.2
Leppert, M.3
Nakamura, Y.4
Muller, U.5
Laiouel, J.-M.6
White, R.7
-
25
-
-
84945446791
-
Analysis of Human Genetic Linkage
-
Press, Baltimore
-
Ott, J. (1991). "Analysis of Human Genetic Linkage," Johns Hopkins Univ. Press, Baltimore.
-
(1991)
Johns Hopkins Univ
-
-
Ott, J.1
-
26
-
-
77958399732
-
Tetranu- cleotide repeat polymorphism at the human myelin basic protein gene (MBP)
-
Polymeropoulos, M. H., Xiao, H., and Merril, C. R. (1992). Tetranu- cleotide repeat polymorphism at the human myelin basic protein gene (MBP). Hum. Mol. Genet. 1: 289.
-
(1992)
Hum. Mol. Genet
, vol.1
, pp. 289
-
-
Polymeropoulos, M.H.1
Xiao, H.2
Merril, C.R.3
-
27
-
-
0027090484
-
Identification and localization of microsatellite markers covering human chromosome 18
-
Rojas, K., Straub, R. E., Kurtz, A., Feder, M., Mewar, R., Gilliam, T. C., and Overhauser, J. (1992). Identification and localization of microsatellite markers covering human chromosome 18. Genomics 14: 1095-1097.
-
(1992)
Genomics
, vol.14
, pp. 1095-1097
-
-
Rojas, K.1
Straub, R.E.2
Kurtz, A.3
Feder, M.4
Mewar, R.5
Gilliam, T.C.6
Overhauser, J.7
-
28
-
-
0026893251
-
Dinucleotide repeat polymorphism at the D18S37 locus
-
Sharma, V., Guo, Z., and Litt, M. (1992). Dinucleotide repeat polymorphism at the D18S37 locus. Hum. Mol. Genet. 1: 289.
-
(1992)
Hum. Mol. Genet
, vol.1
, pp. 289
-
-
Sharma, V.1
Guo, Z.2
Litt, M.3
-
29
-
-
0023119070
-
Assignment of the prealbumin (PALB) gene (familial amyloidotic polyneuropathy) to human chromosome region. 18qll.2-ql2.1. Hum
-
Sparkes, R. S., Sasaki, H., Mohandas, T., Yoshioka, K., Klisak, I., Sakaki, Y., Heinzmann, C., and Simon, M. I. (1987). Assignment of the prealbumin (PALB) gene (familial amyloidotic polyneuropathy) to human chromosome region. 18qll.2-ql2.1. Hum. Genet 75: 151-154.
-
(1987)
Genet
, vol.75
, pp. 151-154
-
-
Sparkes, R.S.1
Sasaki, H.2
Mohandas, T.3
Yoshioka, K.4
Klisak, I.5
Sakaki, Y.6
Heinzmann, C.7
Simon, M.I.8
-
30
-
-
0021821903
-
Involvement of the bcl-2 gene in human follicular lymphoma
-
Tsujimoto, Y., Cossman, J., Jaffe, E., and Croce, C. M. (1985). Involvement of the bcl-2 gene in human follicular lymphoma. Science 228: 1440-1443.
-
(1985)
Science
, vol.228
, pp. 1440-1443
-
-
Tsujimoto, Y.1
Cossman, J.2
Jaffe, E.3
Croce, C.M.4
-
31
-
-
0023748414
-
Genetic alterations during colorectal-tumor development
-
Vogelstein, B., Feaxon, E. R., Hamilton, S. R., Kern, S. E., Preisinger, A. C., Leppert, M., Nakamura, Y., White, R., Smits, A. M., and Bos, J. L. (1988). Genetic alterations during colorectal-tumor development. N. Engl. J. Med. 3 19: 525-532.
-
(1988)
N. Engl. J. Med
, vol.3
, Issue.19
, pp. 525-532
-
-
Vogelstein, B.1
Feaxon, E.R.2
Hamilton, S.R.3
Kern, S.E.4
Preisinger, A.C.5
Leppert, M.6
Nakamura, Y.7
White, R.8
Smits, A.M.9
Bos, J.L.10
-
32
-
-
0022635816
-
I8p- syndrome-. An unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence
-
Vorsanova, S. G., Yurov, Y. B., Alexandrov, I. A., Demidova, I. A., Mitkevich, S. P., and Tirskaia, A. F. (1986). I8p- syndrome-. An unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence. Hum. Genet 72: 185-187.
-
(1986)
Hum. Genet
, vol.72
, pp. 185-187
-
-
Vorsanova, S.G.1
Yurov, Y.B.2
Alexandrov, I.A.3
Demidova, I.A.4
Mitkevich, S.P.5
Tirskaia, A.F.6
-
33
-
-
0025010998
-
Dinucleotide repeat polymorphism at the D18S35 locus
-
Weber, J. L., and May, P. E. (1990a). Dinucleotide repeat polymorphism at the D18S35 locus. Nucleic Acids Res. 18: 6465.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 6465
-
-
Weber, J.L.1
May, P.E.2
-
34
-
-
0025714053
-
Dinucleotide repeat polymorphism at the D18S34 locus
-
Weber, J. L., and May, P. E. (1990b). Dinucleotide repeat polymorphism at the D18S34 locus. Nucleic Acids Res. 18: 2201.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 2201
-
-
Weber, J.L.1
May, P.E.2
-
35
-
-
0026331629
-
Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22
-
Whitcombe, D. M., Carter, N. P., Albertson, D. G., Smith, S. J., Rhodes, D. A., and Cox, T. M. (1991). Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22. Genomics 11: 1152-1154.
-
(1991)
Genomics
, vol.11
, pp. 1152-1154
-
-
Whitcombe, D.M.1
Carter, N.P.2
Albertson, D.G.3
Smith, S.J.4
Rhodes, D.A.5
Cox, T.M.6
-
36
-
-
0025296852
-
Partial trisomy 18 with minimal anomalies: Lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18
-
Wilson, G- N., Heller, K. B., Elterman, R. D., and Schneider, N. R. (1990). Partial trisomy 18 with minimal anomalies: lack of correspondence between phenotypic manifestations and triplicated loci along chromosome 18. Am. J. Med. Genet. 36: 506-510.
-
(1990)
Am. J. Med. Genet
, vol.36
, pp. 506-510
-
-
Wilson, G.-N.1
Heller, K.B.2
Elterman, R.D.3
Schneider, N.R.4
|