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Clinical Genetics|December 8, 2016
PUGS: A novel scale to assess perceptions of uncertainties in genome sequencingB B Biesecker, S W Woolford, W M P Klein, et al.Nature Genetics|October 1, 1995
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsJ P Struewing, D Abeliovich, T Peretz, et al.Breast Cancer Research and Treatment|January 1, 1995
Transcript identification in the BRCA1 candidate regionB L Weber, K J Abel, F J Couch, et al.Nature Genetics|February 1, 1994
A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33-34M T McDonald, K A Papenberg, S Ghosh, et al.Clinical Genetics|February 1, 2018
Disclosure of cardiac variants of uncertain significance results in an exome cohortT A Lawal, K L Lewis, J J Johnston, et al.Journal of the National Cancer Institute|February 26, 1999
Survival after breast cancer in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriersJ S Lee, S Wacholder, J P Struewing, et al.The Journal of Biological Chemistry|October 5, 1988
Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural geneG A Mitchell, J E Looney, L C Brody, et al.Genomics|May 1, 1993
The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YACM T Geraghty, L C Brody, L S Martin, et al.The Journal of Clinical Investigation|February 1, 1988
An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retinaG A Mitchell, L C Brody, J Looney, et al.Human Genetics|September 10, 1999
BRCA1 mutations in African AmericansR C Panguluri, L C Brody, R Modali, et al.Pageof 9