-
1
-
-
0028064998
-
An autosomal locus causing autoimmune disease: Autoimmune polyglandular disease type I assigned to chromosome 21
-
Aaltonen J., Bjorses P., Sandkuijl L., Perheentupa J., Peltonen L. An autosomal locus causing autoimmune disease: Autoimmune polyglandular disease type I assigned to chromosome 21. Nature Genet. 8:1994;83-87.
-
(1994)
Nature Genet.
, vol.8
, pp. 83-87
-
-
Aaltonen, J.1
Bjorses, P.2
Sandkuijl, L.3
Perheentupa, J.4
Peltonen, L.5
-
2
-
-
0025295238
-
Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients
-
Ahonen P., Myllärniemi S., Sipilä I., Perheentupa J. Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients. N. Engl. J. Med. 322:1990;1829-1836.
-
(1990)
N. Engl. J. Med.
, vol.322
, pp. 1829-1836
-
-
Ahonen, P.1
Myllärniemi, S.2
Sipilä, I.3
Perheentupa, J.4
-
3
-
-
0025183708
-
Basic local alignment search tool
-
Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J. Mol. Biol. 215:1990;403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
4
-
-
0027462062
-
Human chromosome 21: Genome mapping and exploration, circa 1993
-
Antonarakis S. E. Human chromosome 21: Genome mapping and exploration, circa 1993. Trends Genet. 9:1993;142-148.
-
(1993)
Trends Genet.
, vol.9
, pp. 142-148
-
-
Antonarakis, S.E.1
-
5
-
-
0029836686
-
Genetic homogeneity of autoimmune polyglandular disease type I
-
Bjorses P., Aaltonen J., Vikman A., Perheentupa J., Ben-Zion G., Chiumello G., Dahl N., Heideman P., Hoorweg-Nijman J. J., Mathivon L., Mullis P. E., Pohl M., Ritzen M., Romeo G., Shapiro M. S., Smith C. S., Solyom J., Zlotogora J., Peltonen L. Genetic homogeneity of autoimmune polyglandular disease type I. Am. J. Hum. Genet. 59:1996;879-886.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 879-886
-
-
Bjorses, P.1
Aaltonen, J.2
Vikman, A.3
Perheentupa, J.4
Ben-Zion, G.5
Chiumello, G.6
Dahl, N.7
Heideman, P.8
Hoorweg-Nijman, J.J.9
Mathivon, L.10
Mullis, P.E.11
Pohl, M.12
Ritzen, M.13
Romeo, G.14
Shapiro, M.S.15
Smith, C.S.16
Solyom, J.17
Zlotogora, J.18
Peltonen, L.19
-
6
-
-
0029883986
-
Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3
-
Bonné-Tamir B., Destefano A. L., Briggs C. E., Adair R., Franklyn B., Weiss S., Korostishevsky M., Frydman M., Baldwin C. T., Farrer L. A. Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3. Am. J. Hum. Genet. 58:1996;1254-1259.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1254-1259
-
-
Bonné-Tamir, B.1
Destefano, A.L.2
Briggs, C.E.3
Adair, R.4
Franklyn, B.5
Weiss, S.6
Korostishevsky, M.7
Frydman, M.8
Baldwin, C.T.9
Farrer, L.A.10
-
7
-
-
0029738953
-
Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping
-
Chen H. M., Chrast R., Rossier C., Morris M. A., Lalioti M. D., Antonarakis S. E. Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping. Genome Res. 6:1996;747-760.
-
(1996)
Genome Res.
, vol.6
, pp. 747-760
-
-
Chen, H.M.1
Chrast, R.2
Rossier, C.3
Morris, M.A.4
Lalioti, M.D.5
Antonarakis, S.E.6
-
8
-
-
0028025053
-
Isolation and mapping of human chromosome 21 cDNA: Progress in constructing a chromosome 21 expression map
-
Cheng J. F., Boyartchuk V., Zhu Y. Isolation and mapping of human chromosome 21 cDNA: Progress in constructing a chromosome 21 expression map. Genomics. 23:1994;75-84.
-
(1994)
Genomics
, vol.23
, pp. 75-84
-
-
Cheng, J.F.1
Boyartchuk, V.2
Zhu, Y.3
-
9
-
-
0026738541
-
Continuum of overlapping clones spanning the entire human chromosome 21q
-
Chumakov I., Rigault P., Guillou S., Ougen P., Billaut A., Guasconi G., Gervy P., LeGall I., Soularue P., Grinas L., Bougueleret L., Bellanne-Chantelot C., Lacroix B., Barillot E., Gesnouin P., Pook S., Vaysseix G., Frelat G., Schmitz A., Sambucy J. L., Bosch A., Estivill X., Weissenbach J., Vignal A., Riethman H., Cox D., Patterson D., Gardiner K., Hattori M., Sakaki Y., Ichikawa H., Ohki M., Le Paslier D., Heilig R., Antonarakis S. E., Cohen D. Continuum of overlapping clones spanning the entire human chromosome 21q. Nature. 359:1992;380-387.
-
(1992)
Nature
, vol.359
, pp. 380-387
-
-
Chumakov, I.1
Rigault, P.2
Guillou, S.3
Ougen, P.4
Billaut, A.5
Guasconi, G.6
Gervy, P.7
Legall, I.8
Soularue, P.9
Grinas, L.10
Bougueleret, L.11
Bellanne-Chantelot, C.12
Lacroix, B.13
Barillot, E.14
Gesnouin, P.15
Pook, S.16
Vaysseix, G.17
Frelat, G.18
Schmitz, A.19
Sambucy, J.L.20
Bosch, A.21
Estivill, X.22
Weissenbach, J.23
Vignal, A.24
Riethman, H.25
Cox, D.26
Patterson, D.27
Gardiner, K.28
Hattori, M.29
Sakaki, Y.30
Ichikawa, H.31
Ohki, M.32
Le Paslier, D.33
Heilig, R.34
Antonarakis, S.E.35
Cohen, D.36
more..
-
10
-
-
0029885038
-
Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q
-
Detera-Wadleigh S. D., Badner J. A., Goldin L. R., Berrettini W. H., Sanders A. R., Rollins D. Y., Turner G., Moses T., Haerian H., Muniec D., Nurnberger J. I., Gershon E. S. Affected-sib-pair analyses reveal support of prior evidence for a susceptibility locus for bipolar disorder, on 21q. Am. J. Hum. Genet. 58:1996;1279-1285.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1279-1285
-
-
Detera-Wadleigh, S.D.1
Badner, J.A.2
Goldin, L.R.3
Berrettini, W.H.4
Sanders, A.R.5
Rollins, D.Y.6
Turner, G.7
Moses, T.8
Haerian, H.9
Muniec, D.10
Nurnberger, J.I.11
Gershon, E.S.12
-
11
-
-
0027320159
-
Sequence-taggedNot
-
Hattori M., Ichikawa H., Ito T., Ohgusu H., Ohishi N., Kano T., Toyoda A., Kuhara S., Ohki M., Sakaki Y. Sequence-taggedNot. Genomics. 17:1993;39-44.
-
(1993)
Genomics
, vol.17
, pp. 39-44
-
-
Hattori, M.1
Ichikawa, H.2
Ito, T.3
Ohgusu, H.4
Ohishi, N.5
Kano, T.6
Toyoda, A.7
Kuhara, S.8
Ohki, M.9
Sakaki, Y.10
-
12
-
-
0027184311
-
ANot
-
Ichikawa H., Hosoda F., Arai Y., Shimizu K., Ohira M., Ohki M. ANot. Nature Genet. 4:1993;361-366.
-
(1993)
Nature Genet.
, vol.4
, pp. 361-366
-
-
Ichikawa, H.1
Hosoda, F.2
Arai, Y.3
Shimizu, K.4
Ohira, M.5
Ohki, M.6
-
13
-
-
0029585732
-
A high-fidelity physical map of human chromosome 21q in yeast artificial chromosomes
-
Korenberg J. R., Chen X.-N., Mitchell S., Fannin S., Gerwehr S., Cohen D., Chumakov I. A high-fidelity physical map of human chromosome 21q in yeast artificial chromosomes. Genome Res. 5:1995;427-443.
-
(1995)
Genome Res.
, vol.5
, pp. 427-443
-
-
Korenberg, J.R.1
Chen, X.-N.2
Mitchell, S.3
Fannin, S.4
Gerwehr, S.5
Cohen, D.6
Chumakov, I.7
-
14
-
-
0029118590
-
A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3
-
Lafrenière R. G., De Jong P., Rouleau G. A. A 405-kb cosmid contig and HindIII restriction map of the progressive myoclonus epilepsy type 1 (EPM1) candidate region in 21q22.3. Genomics. 29:1995;288-290.
-
(1995)
Genomics
, vol.29
, pp. 288-290
-
-
Lafrenière, R.G.1
De Jong, P.2
Rouleau, G.A.3
-
15
-
-
0030586239
-
Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3
-
Lalioti M. D., Chen H. M., Rossier C., Shafaatian R., Reid J. D., Antonarakis S. E. Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3. Genomics. 35:1996;321-327.
-
(1996)
Genomics
, vol.35
, pp. 321-327
-
-
Lalioti, M.D.1
Chen, H.M.2
Rossier, C.3
Shafaatian, R.4
Reid, J.D.5
Antonarakis, S.E.6
-
16
-
-
16944365407
-
Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1)
-
Lalioti M. D., Mirotsou M., Buresi C., Peitsch M. C., Rossier C., Ouazzani R., Baldy-Moulinier M., Bottani A., Malafosse A., Antonarakis S. E. Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1). Am. J. Hum. Genet. 60:1997a;342-351.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 342-351
-
-
Lalioti, M.D.1
Mirotsou, M.2
Buresi, C.3
Peitsch, M.C.4
Rossier, C.5
Ouazzani, R.6
Baldy-Moulinier, M.7
Bottani, A.8
Malafosse, A.9
Antonarakis, S.E.10
-
17
-
-
0030964106
-
Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy
-
Lalioti M. D., Scott H. S., Buresi C., Rossier C., Bottani A., Morris M. A., Malafosse A., Antonarakis S. E. Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy. Nature. 386:1997b;847-851.
-
(1997)
Nature
, vol.386
, pp. 847-851
-
-
Lalioti, M.D.1
Scott, H.S.2
Buresi, C.3
Rossier, C.4
Bottani, A.5
Morris, M.A.6
Malafosse, A.7
Antonarakis, S.E.8
-
18
-
-
0030005755
-
The I.M.A.G.E. Consortium: An integrated molecular analysis of genomes and their expression
-
Lennon G. G., Auffray C., Polymeropoulos M., Soares M. B. The I.M.A.G.E. Consortium: An integrated molecular analysis of genomes and their expression. Genomics. 33:1996;151-152.
-
(1996)
Genomics
, vol.33
, pp. 151-152
-
-
Lennon, G.G.1
Auffray, C.2
Polymeropoulos, M.3
Soares, M.B.4
-
19
-
-
0029127794
-
Localization of 102 exons to a 2.5 Mb region involved in Down syndrome
-
Lucente D., Chen H. M., Shea D., Samec S. N., Rutter M., Chrast R., Rossier C., Buckler A., Antonarakis S. E., McCormick M. K. Localization of 102 exons to a 2.5 Mb region involved in Down syndrome. Hum. Mol. Genet. 4:1995;1305-1311.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1305-1311
-
-
Lucente, D.1
Chen, H.M.2
Shea, D.3
Samec, S.N.4
Rutter, M.5
Chrast, R.6
Rossier, C.7
Buckler, A.8
Antonarakis, S.E.9
McCormick, M.K.10
-
20
-
-
0027308708
-
A linkage map of human chromosome 21: 43 PCR markers at average intervals of 2.5 cM
-
McInnis M. G., Chakravarti A., Blaschak J., Petersen M. B., Sharma V., Avramopoulos D., Blouin J. L., Konig U., Brahe C., Matise T. C., Warren A. C., Talbot C. C. Jr., Van Broeckhoven C., Litt M., Antonarakis S. E. A linkage map of human chromosome 21: 43 PCR markers at average intervals of 2.5 cM. Genomics. 16:1993;562-571.
-
(1993)
Genomics
, vol.16
, pp. 562-571
-
-
McInnis, M.G.1
Chakravarti, A.2
Blaschak, J.3
Petersen, M.B.4
Sharma, V.5
Avramopoulos, D.6
Blouin, J.L.7
Konig, U.8
Brahe, C.9
Matise, T.C.10
Warren, A.C.11
Talbot C.C., Jr.12
Van Broeckhoven, C.13
Litt, M.14
Antonarakis, S.E.15
-
21
-
-
0028787577
-
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome
-
Muenke M., Bone L. J., Mitchell H. F., Hart I., Walton K., Hall-Johnson K., Ippel E. F., Dietz-Band J., Kvaloy K., Fan C. M., Tessier-Lavigne M., Patterson D. Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome. Am. J. Hum. Genet. 57:1995;1074-1079.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 1074-1079
-
-
Muenke, M.1
Bone, L.J.2
Mitchell, H.F.3
Hart, I.4
Walton, K.5
Hall-Johnson, K.6
Ippel, E.F.7
Dietz-Band, J.8
Kvaloy, K.9
Fan, C.M.10
Tessier-Lavigne, M.11
Patterson, D.12
-
22
-
-
0028231476
-
An integrated YAC-overlap and cosmid-pocket map of the human chromosome 21
-
Nizetic D., Gellen L., Hamvas R. M., Mott R., Grigoriev A., Vatcheva R., Zehetner G., Yaspo M. L., Dutriaux A., Lopes C., Delabar J. M., Van Broeckhoven C., Potier M. C., Lehrach H. An integrated YAC-overlap and cosmid-pocket map of the human chromosome 21. Hum. Mol. Genet. 3:1994;759-770.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 759-770
-
-
Nizetic, D.1
Gellen, L.2
Hamvas, R.M.3
Mott, R.4
Grigoriev, A.5
Vatcheva, R.6
Zehetner, G.7
Yaspo, M.L.8
Dutriaux, A.9
Lopes, C.10
Delabar, J.M.11
Van Broeckhoven, C.12
Potier, M.C.13
Lehrach, H.14
-
23
-
-
0027711731
-
Physical mapping of chromosome 21
-
Patterson D., Rahmani Z., Donaldson D., Gardiner K., Jones C. Physical mapping of chromosome 21. Prog. Clin. Biol. Res. 384:1993;33-50.
-
(1993)
Prog. Clin. Biol. Res.
, vol.384
, pp. 33-50
-
-
Patterson, D.1
Rahmani, Z.2
Donaldson, D.3
Gardiner, K.4
Jones, C.5
-
24
-
-
13344269666
-
Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1)
-
Pennacchio L. A., Lehesjoki A. E., Stone N. E., Willour V. L., Virtaneva K., Miao J., D'Amato E., Ramirez L., Faham M., Koskiniemi M., Warrington J. A., Norio R., de la Chapelle A., Cox D. R., Myers R. M. Mutations in the gene encoding cystatin B in progressive myoclonus epilepsy (EPM1). Science. 271:1996;1731-1734.
-
(1996)
Science
, vol.271
, pp. 1731-1734
-
-
Pennacchio, L.A.1
Lehesjoki, A.E.2
Stone, N.E.3
Willour, V.L.4
Virtaneva, K.5
Miao, J.6
D'Amato, E.7
Ramirez, L.8
Faham, M.9
Koskiniemi, M.10
Warrington, J.A.11
Norio, R.12
De La Chapelle, A.13
Cox, D.R.14
Myers, R.M.15
-
25
-
-
0028147991
-
A transcript map of the Down syndrome critical region on chromosome 21
-
Peterson A., Patil N., Robbins C., Wang L., Cox D. R., Myers R. M. A transcript map of the Down syndrome critical region on chromosome 21. Hum. Mol. Genet. 17:1994;1735-1742.
-
(1994)
Hum. Mol. Genet.
, vol.17
, pp. 1735-1742
-
-
Peterson, A.1
Patil, N.2
Robbins, C.3
Wang, L.4
Cox, D.R.5
Myers, R.M.6
-
26
-
-
0025938673
-
Human α-L
-
Scott H. S., Anson D. S., Orsborn A. M., Nelson P. V., Clements P. R., Morris C. P., Hopwood J. J. Human α-L. Proc. Natl. Acad. Sci. USA. 88:1991;9695-9699.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 9695-9699
-
-
Scott, H.S.1
Anson, D.S.2
Orsborn, A.M.3
Nelson, P.V.4
Clements, P.R.5
Morris, C.P.6
Hopwood, J.J.7
-
27
-
-
0028876076
-
Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndrome
-
Scott H. S., Blanch L., Guo X. H., Freeman C., Orsborn A., Baker E., Sutherland G. R., Morris C. P., Hopwood J. J. Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndrome. Nature Genet. 11:1995;465-467.
-
(1995)
Nature Genet.
, vol.11
, pp. 465-467
-
-
Scott, H.S.1
Blanch, L.2
Guo, X.H.3
Freeman, C.4
Orsborn, A.5
Baker, E.6
Sutherland, G.R.7
Morris, C.P.8
Hopwood, J.J.9
-
28
-
-
0030983731
-
Isolation of a human gene (HES1) with homology to anE.coli
-
Scott H. S., Chen H., Rossier C., Lalioti M. D., Antonarakis S. E. Isolation of a human gene (HES1) with homology to anE.coli. Hum. Genet. 99:1997;616-623.
-
(1997)
Hum. Genet.
, vol.99
, pp. 616-623
-
-
Scott, H.S.1
Chen, H.2
Rossier, C.3
Lalioti, M.D.4
Antonarakis, S.E.5
-
29
-
-
0029977272
-
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3
-
Sertié A. L., Quimby M., Moreira E. S., Murray J., Zatz M., Antonarakis S. E., Passos-Bueno M. R. A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. Hum. Mol. Genet. 5:1996;843-847.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 843-847
-
-
Sertié, A.L.1
Quimby, M.2
Moreira, E.S.3
Murray, J.4
Zatz, M.5
Antonarakis, S.E.6
Passos-Bueno, M.R.7
-
30
-
-
0028909271
-
Cosmid assembly and anchoring to human chromosome 21
-
Soeda E., Hou D. X., Osoegawa K., Atsuchi Y., Yamagata T., Shimokawa T., Kishida H., Soeda E., Okano S., Chumakov I., Cohen D., Raff M., Gardiner K., Graw S. L., Patterson D., De Jong P., Ashworth K. L., Slezak T., Carrano A. V. Cosmid assembly and anchoring to human chromosome 21. Genomics. 25:1995;73-84.
-
(1995)
Genomics
, vol.25
, pp. 73-84
-
-
Soeda, E.1
Hou, D.X.2
Osoegawa, K.3
Atsuchi, Y.4
Yamagata, T.5
Shimokawa, T.6
Kishida, H.7
Soeda, E.8
Okano, S.9
Chumakov, I.10
Cohen, D.11
Raff, M.12
Gardiner, K.13
Graw, S.L.14
Patterson, D.15
De Jong, P.16
Ashworth, K.L.17
Slezak, T.18
Carrano, A.V.19
-
31
-
-
0030158571
-
The Staden sequence analysis package
-
Staden R. The Staden sequence analysis package. Mol. Biotechnol. 5:1996;233-241.
-
(1996)
Mol. Biotechnol.
, vol.5
, pp. 233-241
-
-
Staden, R.1
-
32
-
-
19144369837
-
Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy gene
-
Stone N. E., Fan J. B., Willour N., Pennacchio L. A., Warrington J. A., Hu A., de la Chapelle A., Lehesjoki A. E., Cox D. R., Myers R. M. Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy gene. Genome Res. 6:1996;218-225.
-
(1996)
Genome Res.
, vol.6
, pp. 218-225
-
-
Stone, N.E.1
Fan, J.B.2
Willour, N.3
Pennacchio, L.A.4
Warrington, J.A.5
Hu, A.6
De La Chapelle, A.7
Lehesjoki, A.E.8
Cox, D.R.9
Myers, R.M.10
-
33
-
-
0027987228
-
A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3
-
Straub R. E., Lehner T., Luo Y., Loth J. E., Shao W., Sharpe L., Alexander J. R., Das K., Simon R., Fieve R. R. A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3. Nature Genet. 8:1994;291-296.
-
(1994)
Nature Genet.
, vol.8
, pp. 291-296
-
-
Straub, R.E.1
Lehner, T.2
Luo, Y.3
Loth, J.E.4
Shao, W.5
Sharpe, L.6
Alexander, J.R.7
Das, K.8
Simon, R.9
Fieve, R.R.10
-
34
-
-
0029114493
-
CDNA selection from 10 Mb of chromosome 21 DNA: Efficiency in transcriptional mapping and reflections of the genome organization
-
Tassone F., Burkin H., Weissman S. M., Gardiner K. cDNA selection from 10 Mb of chromosome 21 DNA: Efficiency in transcriptional mapping and reflections of the genome organization. Hum. Mol. Genet. 4:1995;1509-1518.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1509-1518
-
-
Tassone, F.1
Burkin, H.2
Weissman, S.M.3
Gardiner, K.4
-
35
-
-
0027968068
-
CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position specific gap penalties and weight matrix choice
-
Thompson J. D., Higgins D. G., Gibson T. J. CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position specific gap penalties and weight matrix choice. Nucleic Acids. Res. 22:1994;4673-4680.
-
(1994)
Nucleic Acids. Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
36
-
-
84995870568
-
Autoantibodies to cytochrome P450scc, P450c17 and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease
-
Uibo R., Aavik E., Peterson P., Perheentupa J., Aranko S., Pelkonen R., Krohn K. Autoantibodies to cytochrome P450scc, P450c17 and P450c21 in autoimmune polyglandular disease types I and II and in isolated Addison's disease. J. Clin. Endocrinol. Metab. 78:1994;323-328.
-
(1994)
J. Clin. Endocrinol. Metab.
, vol.78
, pp. 323-328
-
-
Uibo, R.1
Aavik, E.2
Peterson, P.3
Perheentupa, J.4
Aranko, S.5
Pelkonen, R.6
Krohn, K.7
-
37
-
-
0030070163
-
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan
-
Veske A., Oehlmann R., Younus F., Mohyuddin A., Müller-Myhsok B., Mehdi S. Q., Gal A. Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan. Hum. Mol. Genet. 5:1996;165-168.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 165-168
-
-
Veske, A.1
Oehlmann, R.2
Younus, F.3
Mohyuddin, A.4
Müller-Myhsok, B.5
Mehdi, S.Q.6
Gal, A.7
-
38
-
-
0028964373
-
Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3
-
Yamakawa K., Mitchell S., Hubert R., Chen X.-N., Colbern S., Huo Y.-K., Gadomski C., Kim U.-J., Korenberg J. R. Isolation and characterization of a candidate gene for progressive myoclonus epilepsy on 21q22.3. Hum. Mol. Genet. 4:1995;709-716.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 709-716
-
-
Yamakawa, K.1
Mitchell, S.2
Hubert, R.3
Chen, X.-N.4
Colbern, S.5
Huo, Y.-K.6
Gadomski, C.7
Kim, U.-J.8
Korenberg, J.R.9
-
39
-
-
0029083423
-
Model for a transcript map of human chromosome 21: Isolation of new coding sequences from exon and enriched cDNA libraries
-
Yaspo M. L., Gellen L., Mott R., Korn B., Nizetic D., Poustka A., Lehrach H. Model for a transcript map of human chromosome 21: Isolation of new coding sequences from exon and enriched cDNA libraries. Hum. Mol. Genet. 4:1995;1291-1304.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1291-1304
-
-
Yaspo, M.L.1
Gellen, L.2
Mott, R.3
Korn, B.4
Nizetic, D.5
Poustka, A.6
Lehrach, H.7
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