M. Lee

发表

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.

H. Mefford, M. King, Ming K. Lee, 1997, American journal of human genetics.

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

M. King, Ming K. Lee, B. Huey, 1990, Science.

SeqHelp: a program to analyze molecular sequences utilizing common computational resources.

M. King, M. Lee, E. Lynch, 1998, Genome research.

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

M. King, Ming K. Lee, J. M. Hall, 1991, American journal of human genetics.

22 genes from chromosome 17q21: cloning, sequencing, and characterization of mutations in breast cancer families and tumors.

Ming K. Lee, P. Welcsh, C. Szabo, 1995, Genomics.

The search for BRCA1.

M. King, J. Boyd, C. Szabo, 1994, Cancer research.

Green pigs, red herrings, and a golden hoe: a retrospective on the identification of BRCA1 and the beginning of its characterization.

M. King, P. Dowd, L. Friedman, 1994, Cold Spring Harbor symposia on quantitative biology.

Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1.

L. Hood, M. King, Ming K. Lee, 1996, Genome research.

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

M. King, M. Lee, F. Shen, 1991, American journal of human genetics.

Long terminal repeat and nef gene variants of human immunodeficiency virus type 1 in perinatally infected long-term survivors and rapid progressors.

M. King, C. Rousseau, E. Abrams, 1997, AIDS research and human retroviruses.

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.

M. King, Ming K. Lee, P. Welcsh, 1997, Science.

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

M. King, Ming K. Lee, M. Austin, 1988, Proceedings of the National Academy of Sciences of the United States of America.

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

M. King, Ming K. Lee, C. Morton, 1998, Science.

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

Hanlee P. Ji, M. King, K. Heimdal, 1997, American journal of human genetics.

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

J. Weber, M. King, Ming K. Lee, 1992, American journal of human genetics.

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.

M. King, B. Fernandez, Ming K. Lee, 2001, Human molecular genetics.

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

M. King, E. Goode, Ming K. Lee, 1995, American journal of human genetics.

Rare HRAS alleles and susceptibility to human breast cancer.

M. King, Ming K. Lee, C. Carter, 1990, Genomics.