King MC - Search Results

1

Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.

Shahin H, Walsh T, Rayyan AA, Lee MK, Higgins J, Dickel D, Lewis K, Thompson J, Baker C, Nord AS, Stray S, Gurwitz D, Avraham KB, King MC, Kanaan M. Shahin H, et al. Among authors: king mc. Eur J Hum Genet. 2010 Apr;18(4):407-13. doi: 10.1038/ejhg.2009.190. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888295 Free PMC article.

2

Closing in on a breast cancer gene on chromosome 17q.

Hall JM, Friedman L, Guenther C, Lee MK, Weber JL, Black DM, King MC. Hall JM, et al. Among authors: king mc. Am J Hum Genet. 1992 Jun;50(6):1235-42. Am J Hum Genet. 1992. PMID: 1598904 Free PMC article.

3

Complex segregation analysis of primary hepatocellular carcinoma in Chinese families: interaction of inherited susceptibility and hepatitis B viral infection.

Shen FM, Lee MK, Gong HM, Cai XQ, King MC. Shen FM, et al. Among authors: king mc. Am J Hum Genet. 1991 Jul;49(1):88-93. Am J Hum Genet. 1991. PMID: 1648308 Free PMC article.

4

Possible linkage of the estrogen receptor gene to breast cancer in a family with late-onset disease.

Zuppan P, Hall JM, Lee MK, Ponglikitmongkol M, King MC. Zuppan P, et al. Among authors: king mc. Am J Hum Genet. 1991 Jun;48(6):1065-8. Am J Hum Genet. 1991. PMID: 2035527 Free PMC article.

5

Linkage of early-onset familial breast cancer to chromosome 17q21.

Hall JM, Lee MK, Newman B, Morrow JE, Anderson LA, Huey B, King MC. Hall JM, et al. Among authors: king mc. Science. 1990 Dec 21;250(4988):1684-9. doi: 10.1126/science.2270482. Science. 1990. PMID: 2270482

6

Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families.

Newman B, Austin MA, Lee M, King MC. Newman B, et al. Among authors: king mc. Proc Natl Acad Sci U S A. 1988 May;85(9):3044-8. doi: 10.1073/pnas.85.9.3044. Proc Natl Acad Sci U S A. 1988. PMID: 3362861 Free PMC article.

7

Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families.

Friedman LS, Szabo CI, Ostermeyer EA, Dowd P, Butler L, Park T, Lee MK, Goode EL, Rowell SE, King MC. Friedman LS, et al. Among authors: king mc. Am J Hum Genet. 1995 Dec;57(6):1284-97. Am J Hum Genet. 1995. PMID: 8533757 Free PMC article.

8

BRCA2 in American families with four or more cases of breast or ovarian cancer: recurrent and novel mutations, variable expression, penetrance, and the possibility of families whose cancer is not attributable to BRCA1 or BRCA2.

Schubert EL, Lee MK, Mefford HC, Argonza RH, Morrow JE, Hull J, Dann JL, King MC. Schubert EL, et al. Among authors: king mc. Am J Hum Genet. 1997 May;60(5):1031-40. Am J Hum Genet. 1997. PMID: 9150150 Free PMC article.

9

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.

Lynch ED, Ostermeyer EA, Lee MK, Arena JF, Ji H, Dann J, Swisshelm K, Suchard D, MacLeod PM, Kvinnsland S, Gjertsen BT, Heimdal K, Lubs H, Møller P, King MC. Lynch ED, et al. Among authors: king mc. Am J Hum Genet. 1997 Dec;61(6):1254-60. doi: 10.1086/301639. Am J Hum Genet. 1997. PMID: 9399897 Free PMC article.

10

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, Blumenfeld A, Frydman M, Friedman TB, King MC, Avraham KB. Vahava O, et al. Among authors: king mc. Science. 1998 Mar 20;279(5358):1950-4. doi: 10.1126/science.279.5358.1950. Science. 1998. PMID: 9506947

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