Chamberlain JS - Search Results

1

Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutations.

Couch FJ, Garber J, Kiousis S, Calzone K, Hauser ER, Merajver SD, Frank TS, Boehnke M, Chamberlain JS, Collins FS, et al. Couch FJ, et al. Among authors: chamberlain js. J Natl Cancer Inst Monogr. 1995;(17):9-14. J Natl Cancer Inst Monogr. 1995. PMID: 8573462

2

Characterization of 10 new polymorphic dinucleotide repeats and generation of a high-density microsatellite-based physical map of the BRCA1 region of chromosome 17q21.

Couch FJ, Kiousis S, Castilla LH, Xu J, Chandrasekharappa SC, Chamberlain JS, Collins FS, Weber BL. Couch FJ, et al. Among authors: chamberlain js. Genomics. 1994 Dec;24(3):419-24. doi: 10.1006/geno.1994.1647. Genomics. 1994. PMID: 7713491 Free article.

3

Isolation of tetranucleotide repeat polymorphisms flanking the BRCA1 gene.

Bennett-Baker PE, Kiousis S, Chandrasekharappa SC, King SE, Abel KJ, Collins FS, Weber BL, Chamberlain JS. Bennett-Baker PE, et al. Among authors: chamberlain js. Genomics. 1996 Feb 15;32(1):163-7. doi: 10.1006/geno.1996.0097. Genomics. 1996. PMID: 8786111 Free article.

4

BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis.

Chamberlain JS, Boehnke M, Frank TS, Kiousis S, Xu J, Guo SW, Hauser ER, Norum RA, Helmbold EA, Markel DS, et al. Chamberlain JS, et al. Am J Hum Genet. 1993 Apr;52(4):792-8. Am J Hum Genet. 1993. PMID: 8460646 Free PMC article.

5

Region-specific cosmids and STRPs identified by chromosome microdissection and FISH.

Flejter WL, Bennett-Baker P, Barcroft CL, Kiousis S, Chamberlain JS. Flejter WL, et al. Among authors: chamberlain js. Genomics. 1995 Jan 20;25(2):413-20. doi: 10.1016/0888-7543(95)80041-j. Genomics. 1995. PMID: 7789975

6

Dinucleotide repeat polymorphism at D21S49 (21q22.3).

Bespalova IN, Kiousis S, Chamberlain JS, Burmeister M. Bespalova IN, et al. Among authors: chamberlain js. Hum Mol Genet. 1993 May;2(5):613. doi: 10.1093/hmg/2.5.613-a. Hum Mol Genet. 1993. PMID: 8518810 No abstract available.

7

Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12-q22.

Flejter WL, Kukowska-Latallo JF, Kiousis S, Chandrasekharappa SC, King SE, Chamberlain JS. Flejter WL, et al. Among authors: chamberlain js. Hum Mol Genet. 1993 Jul;2(7):1080. doi: 10.1093/hmg/2.7.1080. Hum Mol Genet. 1993. PMID: 8364555 No abstract available.

8

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M. Towbin JA, et al. Among authors: chamberlain js. Circulation. 1993 Jun;87(6):1854-65. doi: 10.1161/01.cir.87.6.1854. Circulation. 1993. PMID: 8504498

9

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms.

Clemens PR, Fenwick RG, Chamberlain JS, Gibbs RA, de Andrade M, Chakraborty R, Caskey CT. Clemens PR, et al. Among authors: chamberlain js. Am J Hum Genet. 1991 Nov;49(5):951-60. Am J Hum Genet. 1991. PMID: 1928100 Free PMC article.

10

Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20.

Ting CN, Burgess DL, Chamberlain JS, Keith TP, Falls K, Meisler MH. Ting CN, et al. Among authors: chamberlain js. Genomics. 1993 Jun;16(3):698-706. doi: 10.1006/geno.1993.1250. Genomics. 1993. PMID: 8325643 Free article.

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