Suchergebnisse - King, Mary-Claire

Allan C. Wilson (1934–91): In memoriam Mary-Claire King von King, Mary-Claire

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2012 Presidential Address: The Scientist as a Citizen of the World von King, Mary-Claire

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2020 William Allan Award address: genetics as a way of thinking—cultural inheritance from our teachers von King, Mary-Claire

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Abundant novel transcriptional units and unconventional gene pairs on human chromosome 22 von Lipovich, Leonard, King, Mary-Claire

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PCR detection of an MboI polymorphism in the ERBB2 (HER2; NEU) gene on chromosome 17q11.2-q12 von Hall, Jeff M., King, Mary-Claire

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Response to DNA damage of CHEK2 missense mutations in familial breast cancer von Roeb, Wendy, Higgins, Jake, King, Mary-Claire

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Accurate and exact CNV identification from targeted high-throughput sequence data von Nord, Alex S, Lee, Ming, King, Mary-Claire, Walsh, Tom

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SeqHelp: A Program to Analyze Molecular Sequences Utilizing Common Computational Resources von Lee, Ming K., Lynch, Eric D., King, Mary-Claire

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A novel sodium bicarbonate cotransporter-like gene in an ancient duplicated region: SLC4A9 at 5q31 von Lipovich, Leonard, Lynch, Eric D, Lee, Ming K, King, Mary-Claire

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Genetics and Genomics: A Call for Papers von DeAngelis, Catherine D., Fontanarosa, Phil B., King, Mary-Claire, Pasche, Boris

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Genetics and Genomics: A Call for Papers von DeAngelis, Catherine D., Fontanarosa, Phil B., King, Mary-Claire, Pasche, Boris

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Response from Newman, et al von Newmann, Beth, Quesenberry, Charles P., King, Mary-Claire, Selby, Joseph V., Friedman, Gary D.

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Genomic structure of chromosome 17 deletions in BRCA1 associated ovarian cancers von Chisholm, Karen M., Goff, Barbara A., Garcia, Rochelle, King, Mary-Claire, Swisher, Elizabeth M.

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Comparative analysis of cancer genes in the human and chimpanzee genomes von Puente, Xose S, Velasco, Gloria, Gutiérrez-Fernández, Ana, Bertranpetit, Jaume, King, Mary-Claire, López-Otín, Carlos

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A truncating mutation in GPSM2 is associated with recessive nonsyndromic hearing loss von Yariz, Kemal O., Walsh, Tom, Akay, Hatice, Duman, Duygu, Akkaynak, Adil Cinar, King, Mary-Claire, Tekin, Mustafa

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CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes von Walsh, Tom, Casadei, Silvia, Munson, Katherine M, Eng, Mary, Mandell, Jessica B, Gulsuner, Suleyman, King, Mary-Claire

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Spinal Muscular Atrophy with Pontocerebellar Hypoplasia Is Caused by a Mutation in the VRK1 Gene von Renbaum, Paul, Kellerman, Efrat, Jaron, Ranit, Geiger, Dan, Segel, Reeval, Lee, Ming, King, Mary Claire, Levy-Lahad, Ephrat

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Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome von Yariz, Kemal O., Walsh, Tom, Uzak, Asli, Spiliopoulos, Michail, Duman, Duygu, Onalan, Gogsen, King, Mary-Claire, Tekin, Mustafa

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A Genomewide Screen for Suppressors of Alu-Mediated Rearrangements Reveals a Role for PIF1 von Chisholm, Karen M., Aubert, Sarah D., Freese, Krister P., Zakian, Virginia A., King, Mary-Claire, Welcsh, Piri L.

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FAM111B MUTATION IS ASSOCIATED WITH INHERITED EXOCRINE PANCREATIC DYSFUNCTION von Seo, Aaron, Walsh, Tom, Lee, Ming, Ho, Phoenix, Hsu, Evelyn Kanyu, Sidbury, Robert, King, Mary-Claire, Shimamura, Akiko

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