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Publications by Mary-Claire King
Gene Discovery for Complex Traits: Lessons From Africa
Cell
Biochemistry
Genetics
Molecular Biology
A Recurrent Germline PAX5 Mutation Confers Susceptibility to Pre-B Cell Acute Lymphoblastic Leukemia
Nature Genetics
Genetics
Germline ETV6 Mutations in Familial Thrombocytopenia and Hematologic Malignancy
Nature Genetics
Genetics
Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas
Clinical Cancer Research
Cancer Research
Oncology
Genomic Analysis of Inherited Breast Cancer Among Palestinian Women: Genetic Heterogeneity and a Founder Mutation in TP53
International Journal of Cancer
Cancer Research
Oncology
Five Novel Loci for Inherited Hearing Loss Mapped by SNP-based Homozygosity Profiles in Palestinian Families
European Journal of Human Genetics
Genetics
Profound, Prelingual Nonsyndromic Deafness Maps to Chromosome 10q21 and Is Caused by a Novel Missense Mutation in the Usher Syndrome Type IF Gene PCDH15
European Journal of Human Genetics
Genetics
