-
2
-
-
0026318628
-
Molecular genetic considerations in osteosarcoma
-
Hansen, M. F. Molecular genetic considerations in osteosarcoma. Clin. Orthop. Relat. Res., 270: 237-246, 1991.
-
(1991)
Clin. Orthop. Relat. Res.
, vol.270
, pp. 237-246
-
-
Hansen, M.F.1
-
3
-
-
0025855326
-
Complete association of loss of heterozygosity of chromosomes 13 and 17 in osteosarcoma
-
Scheffer, H., Kruize, Y. C., Osinga, J., Kuiken, G., Oosterhuis, J. W., Leeuw, J. A., Schraffordt-Koops, H., and Buys, C. H. Complete association of loss of heterozygosity of chromosomes 13 and 17 in osteosarcoma. Cancer Genet. Cytogenet., 53: 45-55, 1991.
-
(1991)
Cancer Genet. Cytogenet.
, vol.53
, pp. 45-55
-
-
Scheffer, H.1
Kruize, Y.C.2
Osinga, J.3
Kuiken, G.4
Oosterhuis, J.W.5
Leeuw, J.A.6
Schraffordt-Koops, H.7
Buys, C.H.8
-
4
-
-
0023777950
-
Chromosomal reorganization for the expression of recessive mutation of retinoblastoma susceptibility gene in the development of osteosarcoma
-
Toguchida, J., Ishizaki, K., Sasaki, M. S., Ikenaga, M., Sugimoto, M., Kotoura, Y., and Yamamuro, T. Chromosomal reorganization for the expression of recessive mutation of retinoblastoma susceptibility gene in the development of osteosarcoma. Cancer Res., 48: 3939-3943, 1988.
-
(1988)
Cancer Res.
, vol.48
, pp. 3939-3943
-
-
Toguchida, J.1
Ishizaki, K.2
Sasaki, M.S.3
Ikenaga, M.4
Sugimoto, M.5
Kotoura, Y.6
Yamamuro, T.7
-
5
-
-
0024332918
-
Assignment of common allele loss in osteosarcoma to the subregion 17p13
-
Toguchida, J., Ishizaki, K., Nakamura, Y., Sasaki, M. S., Ikenaga, M., Kato, M., Sugimoto, M., Kotoura, Y., and Yamamuro, T. Assignment of common allele loss in osteosarcoma to the subregion 17p13. Cancer Res., 49: 6247-6251, 1989.
-
(1989)
Cancer Res.
, vol.49
, pp. 6247-6251
-
-
Toguchida, J.1
Ishizaki, K.2
Nakamura, Y.3
Sasaki, M.S.4
Ikenaga, M.5
Kato, M.6
Sugimoto, M.7
Kotoura, Y.8
Yamamuro, T.9
-
6
-
-
0022402666
-
Osteosarcoma and retinoblastoma: A shared chromosomal mechanism revealing recessive predisposition
-
Hansen, M. F., Koufos, A., Gallie, B. L., Phillips, R. A., Fodstad, O., Brogger, A., Gedde-Dahl, T., and Cavenee, W. K. Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition. Proc. Natl. Acad. Sci. USA, 82: 6216-6220, 1985.
-
(1985)
Proc. Natl. Acad. Sci. USA
, vol.82
, pp. 6216-6220
-
-
Hansen, M.F.1
Koufos, A.2
Gallie, B.L.3
Phillips, R.A.4
Fodstad, O.5
Brogger, A.6
Gedde-Dahl, T.7
Cavenee, W.K.8
-
7
-
-
0025648762
-
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome
-
Srivastava, S., Zou, Z. Q., Pirollo, K., Blattner, W., and Chang, E. H. Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. Nature (Lond.), 348: 747-749, 1990.
-
(1990)
Nature (Lond.)
, vol.348
, pp. 747-749
-
-
Srivastava, S.1
Zou, Z.Q.2
Pirollo, K.3
Blattner, W.4
Chang, E.H.5
-
8
-
-
0026548948
-
Germ-line and somatic p53 gene mutations in multifocal osteogenic sarcoma
-
Iavarone, A., Matthay, K. K., Steinkirchner, T. M., and Israel, M. A. Germ-line and somatic p53 gene mutations in multifocal osteogenic sarcoma. Proc. Natl. Acad. Sci. USA, 89: 4207-4209, 1992.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 4207-4209
-
-
Iavarone, A.1
Matthay, K.K.2
Steinkirchner, T.M.3
Israel, M.A.4
-
9
-
-
0028350959
-
Germline mutations of the p53 tumor suppressor gene in children with osteosarcoma
-
McIntyre, J. F., Smith-Sorensen, B., Friend, S. H., Kassell, J., Borresen, A. L., Yan, Y. X., Russo, C., Sato, J., Barbier, N., Miser, J., Malkin, D., and Gebhardt, M. C. Germline mutations of the p53 tumor suppressor gene in children with osteosarcoma. J. Clin. Oncol., 12: 925-930, 1994.
-
(1994)
J. Clin. Oncol.
, vol.12
, pp. 925-930
-
-
McIntyre, J.F.1
Smith-Sorensen, B.2
Friend, S.H.3
Kassell, J.4
Borresen, A.L.5
Yan, Y.X.6
Russo, C.7
Sato, J.8
Barbier, N.9
Miser, J.10
Malkin, D.11
Gebhardt, M.C.12
-
10
-
-
34547384728
-
A germline missense mutation in exon 10 of the human p53 gene
-
in press
-
Luca, J. W., Strong, L. C., and Hansen, M. F. A germline missense mutation in exon 10 of the human p53 gene. Hum. Mut., in press, 1996.
-
(1996)
Hum. Mut.
-
-
Luca, J.W.1
Strong, L.C.2
Hansen, M.F.3
-
11
-
-
0020518746
-
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
-
Cavenee, W. K., Dryja, T. P., Phillips, R. A., Benedict, W. F., Godbout, R., Gallie, B. L., Murphree, A. L., Strong, L. C., and White, R. L. Expression of recessive alleles by chromosomal mechanisms in retinoblastoma. Nature (Lond.), 305: 779-784, 1983.
-
(1983)
Nature (Lond.)
, vol.305
, pp. 779-784
-
-
Cavenee, W.K.1
Dryja, T.P.2
Phillips, R.A.3
Benedict, W.F.4
Godbout, R.5
Gallie, B.L.6
Murphree, A.L.7
Strong, L.C.8
White, R.L.9
-
12
-
-
0023584218
-
Genetics of cancer predisposition
-
Hansen, M. F., and Cavenee, W. K. Genetics of cancer predisposition. Cancer Res., 47: 5518-5527, 1987.
-
(1987)
Cancer Res.
, vol.47
, pp. 5518-5527
-
-
Hansen, M.F.1
Cavenee, W.K.2
-
13
-
-
0023936804
-
Tumor suppressors: Recessive mutations that lead to cancer
-
Hansen, M. F., and Cavenee, W. K. Tumor suppressors: recessive mutations that lead to cancer. Cell, 53: 173-174, 1988.
-
(1988)
Cell
, vol.53
, pp. 173-174
-
-
Hansen, M.F.1
Cavenee, W.K.2
-
14
-
-
0024514647
-
Allelotype of colorectal carcinomas
-
Vogelstein, B., Fearon, E. R., Kern, S. E., Hamilton, S. R., Preisinger, A. C., Nakamura, Y., and White, R. Allelotype of colorectal carcinomas. Science (Washington DC), 244: 207-211, 1989.
-
(1989)
Science (Washington DC)
, vol.244
, pp. 207-211
-
-
Vogelstein, B.1
Fearon, E.R.2
Kern, S.E.3
Hamilton, S.R.4
Preisinger, A.C.5
Nakamura, Y.6
White, R.7
-
15
-
-
0025941543
-
Allelotype of human ovarian cancer
-
Sato, T., Saito, H., Morita, R., Koi, S., Lee, J. H., and Nakamura, Y. Allelotype of human ovarian cancer. Cancer Res., 51: 5118-5122, 1991.
-
(1991)
Cancer Res.
, vol.51
, pp. 5118-5122
-
-
Sato, T.1
Saito, H.2
Morita, R.3
Koi, S.4
Lee, J.H.5
Nakamura, Y.6
-
16
-
-
0028009282
-
Allelotype of human bladder cancer
-
Knowles, M. A., Elder, P. A., Williamson, M., Cairns, J. P., Shaw, M. E., and Law, M. G. Allelotype of human bladder cancer. Cancer Res., 54: 531-538, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 531-538
-
-
Knowles, M.A.1
Elder, P.A.2
Williamson, M.3
Cairns, J.P.4
Shaw, M.E.5
Law, M.G.6
-
17
-
-
0028048475
-
Allelotype analysis of cervical carcinoma
-
Mitra, A. B., Murty, V. V., Li, R. G., Pratap, M., Luthra, U. K., and Chaganti, R. S. Allelotype analysis of cervical carcinoma. Cancer Res., 54: 4481-4487, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 4481-4487
-
-
Mitra, A.B.1
Murty, V.V.2
Li, R.G.3
Pratap, M.4
Luthra, U.K.5
Chaganti, R.S.6
-
18
-
-
0026647228
-
Allelotype analysis in osteosarcomas: Frequent allele loss on 3q, 13q, 17p, and 18q
-
Yamaguchi, T., Toguchida, J., Yamamuro, T., Kotoura, Y., Takada, N., Kawaguchi, N., Kaneko, Y., Nakamura, Y., Sasaki, M., and Ishizaki, K. Allelotype analysis in osteosarcomas: frequent allele loss on 3q, 13q, 17p, and 18q. Cancer Res., 52: 2419-2423, 1992.
-
(1992)
Cancer Res.
, vol.52
, pp. 2419-2423
-
-
Yamaguchi, T.1
Toguchida, J.2
Yamamuro, T.3
Kotoura, Y.4
Takada, N.5
Kawaguchi, N.6
Kaneko, Y.7
Nakamura, Y.8
Sasaki, M.9
Ishizaki, K.10
-
19
-
-
0028225322
-
Allelotype of pancreatic adenocarcinoma
-
Seymour, A. B., Hruban, R. H., Redston, M., Caldas, C., Powell, S. M., Kinzler, K. W., Yeo, C. J., and Kern, S. E. Allelotype of pancreatic adenocarcinoma. Cancer Res., 54: 2761-2764, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 2761-2764
-
-
Seymour, A.B.1
Hruban, R.H.2
Redston, M.3
Caldas, C.4
Powell, S.M.5
Kinzler, K.W.6
Yeo, C.J.7
Kern, S.E.8
-
20
-
-
0028362513
-
Allelotype study of esophageal carcinoma
-
Aoki, T., Mori, T., Du, X., Nisihira, T., Matsubara, T., and Nakamura, Y. Allelotype study of esophageal carcinoma. Genes Chromosomes Cancer, 10: 177-182, 1994.
-
(1994)
Genes Chromosomes Cancer
, vol.10
, pp. 177-182
-
-
Aoki, T.1
Mori, T.2
Du, X.3
Nisihira, T.4
Matsubara, T.5
Nakamura, Y.6
-
21
-
-
0028350523
-
Allelotype of head and neck squamous cell carcinoma
-
Nawroz, H., van der Riet, P., Hruban, R. H., Koch, W., Ruppert, J. M., and Sidransky, D. Allelotype of head and neck squamous cell carcinoma. Cancer Res., 54: 1152- 1155, 1994.
-
(1994)
Cancer Res.
, vol.54
, pp. 1152-1155
-
-
Nawroz, H.1
Van der Riet, P.2
Hruban, R.H.3
Koch, W.4
Ruppert, J.M.5
Sidransky, D.6
-
22
-
-
0019190556
-
Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14
-
Sparkes, R. S., Sparkes, M. C., Wilson, M. G., Towner, J. W., Benedict, W. F., Murphree, A. L., and Yunis, J. J. Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14. Science (Washington DC), 208: 1042-1044, 1980.
-
(1980)
Science (Washington DC)
, vol.208
, pp. 1042-1044
-
-
Sparkes, R.S.1
Sparkes, M.C.2
Wilson, M.G.3
Towner, J.W.4
Benedict, W.F.5
Murphree, A.L.6
Yunis, J.J.7
-
23
-
-
0024490717
-
Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus
-
Higgins, M. J., Hansen, M. F., Cavenee, W. K., and Lalande, M. Molecular detection of chromosomal translocations that disrupt the putative retinoblastoma susceptibility locus. Mol. Cell. Biol. 9: 1-5, 1989.
-
(1989)
Mol. Cell. Biol.
, vol.9
, pp. 1-5
-
-
Higgins, M.J.1
Hansen, M.F.2
Cavenee, W.K.3
Lalande, M.4
-
24
-
-
0022646788
-
Localization of gene for human p53 tumour antigen to band 17p13
-
Isobe, M., Emanuel, B. S., Givol, D., Oren, M., and Croce, C. M. Localization of gene for human p53 tumour antigen to band 17p13. Nature (Lond.), 320: 84-85, 1986.
-
(1986)
Nature (Lond.)
, vol.320
, pp. 84-85
-
-
Isobe, M.1
Emanuel, B.S.2
Givol, D.3
Oren, M.4
Croce, C.M.5
-
25
-
-
0344246051
-
The gene for human p53 cellular tumor antigen is located on chromosome 17 short arm (17p13)
-
McBride, O. W., Merry, D., and Givol, D. The gene for human p53 cellular tumor antigen is located on chromosome 17 short arm (17p13). Proc. Natl. Acad. Sci. USA, 83: 130-134, 1986.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 130-134
-
-
McBride, O.W.1
Merry, D.2
Givol, D.3
-
26
-
-
0022623436
-
Human p53 gene localized to short arm of chromosome 17
-
Miller, C., Mohandas, T., Wolf, D., Prokocimer, M., Rotter, V., and Koeffler, H. P. Human p53 gene localized to short arm of chromosome 17. Nature (Lond.), 319: 783-784, 1986.
-
(1986)
Nature (Lond.)
, vol.319
, pp. 783-784
-
-
Miller, C.1
Mohandas, T.2
Wolf, D.3
Prokocimer, M.4
Rotter, V.5
Koeffler, H.P.6
-
27
-
-
0023226545
-
Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping
-
Scrable, H. J., Witte, D. P., Lampkin, B. C., and Cavenee, W. K. Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping. Nature (Lond.), 329: 645-647, 1987.
-
(1987)
Nature (Lond.)
, vol.329
, pp. 645-647
-
-
Scrable, H.J.1
Witte, D.P.2
Lampkin, B.C.3
Cavenee, W.K.4
-
28
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller, S. A., Dykes, D. D., and Polesky, H. F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res., 16: 1215, 1988.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
29
-
-
0024582686
-
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
-
Weber, J. L., and May, P. E. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. Hum. Genet., 44: 388-396, 1989.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 388-396
-
-
Weber, J.L.1
May, P.E.2
-
30
-
-
0025815970
-
Tetranucleotide repeat polymorphism at the ACPP locus
-
Doak, S., Jordan, S., McWilliam, P., and Humphries, P. Tetranucleotide repeat polymorphism at the ACPP locus. Nucleic Acids Res., 19: 4793, 1991.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 4793
-
-
Doak, S.1
Jordan, S.2
McWilliam, P.3
Humphries, P.4
-
31
-
-
0028247562
-
Report and abstracts of the Fourth International Workshop on Human Chromosome 3 Mapping
-
Naylor, S. L., Buys, C. H., and Carritt, B. Report and abstracts of the Fourth International Workshop on Human Chromosome 3 Mapping. Cytogenet. Cell Genet., 65: 2-50, 1994.
-
(1994)
Cytogenet. Cell Genet.
, vol.65
, pp. 2-50
-
-
Naylor, S.L.1
Buys, C.H.2
Carritt, B.3
-
32
-
-
0028231090
-
The 1993-94 Genethon human genetic linkage map
-
Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. The 1993-94 Genethon human genetic linkage map. Nat. Genet., 7: 246-339, 1994.
-
(1994)
Nat. Genet.
, vol.7
, pp. 246-339
-
-
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
-
33
-
-
0025772537
-
Dinucleotide repeat polymorphism in human GLUT2/liver facilitative glucose transporter gene on chromosome 3
-
Granqvist, M., Xiang, K., Seino, M., Fukumoto, H., and Bell, G. I. Dinucleotide repeat polymorphism in human GLUT2/liver facilitative glucose transporter gene on chromosome 3. Nucleic Acids Res., 19: 4791, 1991.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 4791
-
-
Granqvist, M.1
Xiang, K.2
Seino, M.3
Fukumoto, H.4
Bell, G.I.5
-
34
-
-
0028936830
-
Report of the Fifth International Workshop on Human Chromosome 3 Mapping 1994
-
Smith, D. I., Glover, T. W., Gemmill, R., Drabkin, H., O'Connell, P., and Naylor, S. L. Report of the Fifth International Workshop on Human Chromosome 3 Mapping 1994. Cytogenet. Cell Genet., 65: 126-146, 1995.
-
(1995)
Cytogenet. Cell Genet.
, vol.65
, pp. 126-146
-
-
Smith, D.I.1
Glover, T.W.2
Gemmill, R.3
Drabkin, H.4
O'Connell, P.5
Naylor, S.L.6
-
35
-
-
0004136246
-
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory
-
Sambrook, J., Fritsch, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual, Ed. 2, pp. 6.12-6.45. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory, 1989.
-
(1989)
Molecular Cloning: A Laboratory Manual, Ed. 2
, pp. 612-645
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
36
-
-
0025898874
-
A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome
-
Ireland, M., English, C., Cross, I., Houlsby, W. T., and Burn, J. A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome. J. Med. Genet., 28: 639-640, 1991.
-
(1991)
J. Med. Genet.
, vol.28
, pp. 639-640
-
-
Ireland, M.1
English, C.2
Cross, I.3
Houlsby, W.T.4
Burn, J.5
-
37
-
-
0028158546
-
Partial trisomy 3q causing mild Cornelia de Lange phenotype
-
Holder, S. E., Grimsley, L. M., Palmer, R. W., Butler, L. J., and Baraitser, M. Partial trisomy 3q causing mild Cornelia de Lange phenotype. J. Med. Genet., 31: 150-152, 1994.
-
(1994)
J. Med. Genet.
, vol.31
, pp. 150-152
-
-
Holder, S.E.1
Grimsley, L.M.2
Palmer, R.W.3
Butler, L.J.4
Baraitser, M.5
-
38
-
-
0027365303
-
Radiological features in Brachmann-de Lange syndrome
-
Braddock, S. R., Lachman, R. S., Stoppenhagen, C. C., Carey, J. C., Ireland, M., Moeschler, J. B., Cunniff, C., and Graham, J. M., Jr. Radiological features in Brachmann-de Lange syndrome. Am. J. Med. Genet., 47: 1006-1013, 1993.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 1006-1013
-
-
Braddock, S.R.1
Lachman, R.S.2
Stoppenhagen, C.C.3
Carey, J.C.4
Ireland, M.5
Moeschler, J.B.6
Cunniff, C.7
Graham Jr., J.M.8
-
39
-
-
0027423908
-
Brachmann-de Lange syndrome: Delineation of the clinical phenotype
-
Ireland, M., Donnai, D., and Burn, J. Brachmann-de Lange syndrome: delineation of the clinical phenotype. Am. J. Med. Genet., 47: 959-964, 1993.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 959-964
-
-
Ireland, M.1
Donnai, D.2
Burn, J.3
-
40
-
-
0017144546
-
Epidemiology of Cornelia de Lange's syndrome
-
Beck, B. Epidemiology of Cornelia de Lange's syndrome. Acta Paediat. Scand., 65: 631-638, 1976.
-
(1976)
Acta Paediat. Scand.
, vol.65
, pp. 631-638
-
-
Beck, B.1
-
41
-
-
0022786624
-
Familial occurrence of Brachmann-de Lange syndrome
-
Bankier, A., Haan, E., and Birrell, R. Familial occurrence of Brachmann-de Lange syndrome. Am. J. Med. Genet., 25: 163-165, 1986.
-
(1986)
Am. J. Med. Genet.
, vol.25
, pp. 163-165
-
-
Bankier, A.1
Haan, E.2
Birrell, R.3
-
42
-
-
0022006820
-
Brachmann-de Lange syndrome: Evidence for autosomal dominant inheritance
-
Robinson, L. K., Wolfsberg, E., and Jones, K. L., Brachmann-de Lange syndrome: evidence for autosomal dominant inheritance. Am. J. Med. Genet., 22: 109-115, 1985.
-
(1985)
Am. J. Med. Genet.
, vol.22
, pp. 109-115
-
-
Robinson, L.K.1
Wolfsberg, E.2
Jones, K.L.3
-
43
-
-
0027482013
-
Familial Brachmann-de Lange syndrome: Further evidence for autosomal dominant inheritance and review of the literature
-
Feingold, M., and Lin, A. E., Familial Brachmann-de Lange syndrome: further evidence for autosomal dominant inheritance and review of the literature. Am. J. Med. Genet., 47: 1064-1067, 1993.
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 1064-1067
-
-
Feingold, M.1
Lin, A.E.2
-
44
-
-
84907115591
-
Aniridia, Wilms' tumor and human chromosome 11
-
Bickmore, W. A., and Hastie, N. D., Aniridia, Wilms' tumor and human chromosome 11. Ophthalmic Paediat. Genet., 10: 229-248, 1989.
-
(1989)
Ophthalmic Paediat. Genet.
, vol.10
, pp. 229-248
-
-
Bickmore, W.A.1
Hastie, N.D.2
-
45
-
-
0025945993
-
The distal region of 11p13 and associated genetic diseases
-
Mannens, M., Hoovers, J. M., Bleeker-Wagemakers, E. M., Redeker, E., Bliek, J., Overbeeke-Melkert, M., Saunders, G., Williams, B., van Heyningen, V., Junien, C., and Hastie, N. The distal region of 11p13 and associated genetic diseases. Genomics, 11: 284-293, 1991.
-
(1991)
Genomics
, vol.11
, pp. 284-293
-
-
Mannens, M.1
Hoovers, J.M.2
Bleeker-Wagemakers, E.M.3
Redeker, E.4
Bliek, J.5
Overbeeke-Melkert, M.6
Saunders, G.7
Williams, B.8
Van Heyningen, V.9
Junien, C.10
Hastie, N.11
-
46
-
-
0026602124
-
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
-
Tassabehji, M., Read, A. P., Newton, V. E., Harris, R., Balling, R., Gruss, P., and Strachan, T. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene. Nature (Lond.), 355: 635-636, 1992.
-
(1992)
Nature (Lond.)
, vol.355
, pp. 635-636
-
-
Tassabehji, M.1
Read, A.P.2
Newton, V.E.3
Harris, R.4
Balling, R.5
Gruss, P.6
Strachan, T.7
-
47
-
-
0026584439
-
An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
-
Baldwin, C. T., Hoth, C. F., Amos, J. A., da-Silva, E. O., and Milunsky, A. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature (Lond.), 355: 637-638, 1992.
-
(1992)
Nature (Lond.)
, vol.355
, pp. 637-638
-
-
Baldwin, C.T.1
Hoth, C.F.2
Amos, J.A.3
Da-Silva, E.O.4
Milunsky, A.5
-
48
-
-
0027439075
-
Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)
-
Hoth, C. F., Milunsky, A., Lipsky, N., Sheffer, R., Clarren, S. K., and Baldwin, C. T. Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I). Am. J. Hum. Genet., 52: 455-462, 1993.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 455-462
-
-
Hoth, C.F.1
Milunsky, A.2
Lipsky, N.3
Sheffer, R.4
Clarren, S.K.5
Baldwin, C.T.6
-
49
-
-
0027518348
-
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2
-
Tassabehji, M., Read, A. P., Newton, V. E., Patton, M., Gruss, P., Harris, R., and Strachan, T. Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2. Nat. Genet., 3: 26-30, 1993.
-
(1993)
Nat. Genet.
, vol.3
, pp. 26-30
-
-
Tassabehji, M.1
Read, A.P.2
Newton, V.E.3
Patton, M.4
Gruss, P.5
Harris, R.6
Strachan, T.7
-
50
-
-
0028289314
-
Mutations in PAX3 associated with Waardenburg syndrome type I
-
Baldwin, C. T., Lipsky, N. R., Hoth, C. F., Cohen, T., Mamuya, W., and Milunsky, A. Mutations in PAX3 associated with Waardenburg syndrome type I. Hum. Mut., 3: 205-211, 1994.
-
(1994)
Hum. Mut.
, vol.3
, pp. 205-211
-
-
Baldwin, C.T.1
Lipsky, N.R.2
Hoth, C.F.3
Cohen, T.4
Mamuya, W.5
Milunsky, A.6
-
51
-
-
0027534945
-
Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma
-
Barr, F. G., Galili, N., Holick, J., Biegel, J. A., Rovera, G., and Emanuel, B. S. Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma. Nat. Genet., 3: 113-117, 1993.
-
(1993)
Nat. Genet.
, vol.3
, pp. 113-117
-
-
Barr, F.G.1
Galili, N.2
Holick, J.3
Biegel, J.A.4
Rovera, G.5
Emanuel, B.S.6
-
52
-
-
0027521658
-
Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma
-
Galili, N., Davis, R. J., Fredericks, W. J., Mukhopadhyay, S., Rauscher, F. J. d., Emanuel, B. S., Rovera, G., and Barr, F. G. Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma. Nat. Genet., 5: 230-235, 1993.
-
(1993)
Nat. Genet.
, vol.5
, pp. 230-235
-
-
Galili, N.1
Davis, R.J.2
Fredericks, W.J.3
Mukhopadhyay, S.4
Rauscher, F.J.D.5
Emanuel, B.S.6
Rovera, G.7
Barr, F.G.8
|