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L C Brody

Showing results (51-60 of 63) with videos related to

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Journal of Medical Genetics|December 19, 2001
Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1C Eng, L C Brody, T M Wagner, et al.
Somatic Cell and Molecular Genetics|September 1, 1995
Localization of the human homolog of the yeast cell division control 27 gene (CDC27) proximal to ITGB3 on human chromosome 17q21.3P P Ho, F J Couch, L C Brody, et al.
Genomics|January 1, 1995
A YAC-, P1-, and cosmid-based physical map of the BRCA1 region on chromosome 17q21F J Couch, L H Castilla, J Xu, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in FinnsG A Mitchell, L C Brody, I Sipila, et al.
Genomics|January 1, 1995
Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17L C Brody, K J Abel, L H Castilla, et al.
Nature Genetics|December 1, 1994
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancerL H Castilla, F J Couch, M R Erdos, et al.
Molecular Genetics and Metabolism|August 13, 1999
Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defectsL C Brody, P J Baker, P S Chines, et al.
Nature Genetics|October 1, 1996
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%C Oddoux, J P Struewing, C M Clayton, et al.
Journal of Thrombosis and Haemostasis : JTH|July 1, 2016
Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearanceA B Ozel, B McGee, D Siemieniak, et al.
Journal of Medical Genetics|June 26, 2010
Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defectsF Pangilinan, A Mitchell, J VanderMeer, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|December 19, 2001
Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1C Eng, L C Brody, T M Wagner, et al.
Somatic Cell and Molecular Genetics|September 1, 1995
Localization of the human homolog of the yeast cell division control 27 gene (CDC27) proximal to ITGB3 on human chromosome 17q21.3P P Ho, F J Couch, L C Brody, et al.
Genomics|January 1, 1995
A YAC-, P1-, and cosmid-based physical map of the BRCA1 region on chromosome 17q21F J Couch, L H Castilla, J Xu, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1989
At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in FinnsG A Mitchell, L C Brody, I Sipila, et al.
Genomics|January 1, 1995
Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17L C Brody, K J Abel, L H Castilla, et al.
Nature Genetics|December 1, 1994
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancerL H Castilla, F J Couch, M R Erdos, et al.
Molecular Genetics and Metabolism|August 13, 1999
Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defectsL C Brody, P J Baker, P S Chines, et al.
Nature Genetics|October 1, 1996
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%C Oddoux, J P Struewing, C M Clayton, et al.
Journal of Thrombosis and Haemostasis : JTH|July 1, 2016
Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearanceA B Ozel, B McGee, D Siemieniak, et al.
Journal of Medical Genetics|June 26, 2010
Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defectsF Pangilinan, A Mitchell, J VanderMeer, et al.
Pageof 7