D T Bishop|S L Sherman - JoVE Visualize

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Clinical Genetics|November 22, 2008

Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome ProjectsS B Freeman, C P Torfs, P A Romitti, et al.

Genetic Epidemiology|September 5, 1998

Testing for contributions of mitochondrial DNA mutations to complex diseasesF Sun, A E Ashley-Koch, L K Durham, et al.

European Journal of Cancer (Oxford, England : 1990)|January 1, 1994

Intron splice acceptor site sequence variation in the hereditary non-polyposis colorectal cancer gene hMSH2N R Hall, G R Taylor, P J Finan, et al.

Hormone Research in Paediatrics|September 4, 2010

Associations of progesterone receptor polymorphisms with age at menarche and menstrual cycle lengthK C Taylor, C M Small, M P Epstein, et al.

Nature Genetics|November 1, 1992

Human genes containing polymorphic trinucleotide repeatsG J Riggins, L K Lokey, J L Chastain, et al.

Journal of Medical Genetics|February 1, 2008

Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test batteryE G Allen, J Juncos, R Letz, et al.

Human Molecular Genetics|September 1, 1995

Candidate regions for a testicular cancer susceptibility geneM G Leahy, S Tonks, J H Moses, et al.

Human Molecular Genetics|September 1, 1994

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombinationS L Sherman, M B Petersen, S B Freeman, et al.

Clinical Genetics|August 1, 1986

Segregation analysis of balanced pericentric inversions in pedigree dataS L Sherman, L Iselius, P Gallano, et al.

Human Heredity|May 1, 1993

Methodological issues in linkage analyses for psychiatric disorders: secular trends, assortative mating, bilineal pedigrees. Report of the MacArthur Foundation Network I Task Force on Methodological IssuesM A Spence, D T Bishop, M Boehnke, et al.

Pageof 23

Showing results (151-160 of 222) with videos related to

Sort By:

Pageof 23

Clinical Genetics|November 22, 2008

Congenital gastrointestinal defects in Down syndrome: a report from the Atlanta and National Down Syndrome ProjectsS B Freeman, C P Torfs, P A Romitti, et al.

Genetic Epidemiology|September 5, 1998

Testing for contributions of mitochondrial DNA mutations to complex diseasesF Sun, A E Ashley-Koch, L K Durham, et al.

European Journal of Cancer (Oxford, England : 1990)|January 1, 1994

Intron splice acceptor site sequence variation in the hereditary non-polyposis colorectal cancer gene hMSH2N R Hall, G R Taylor, P J Finan, et al.

Hormone Research in Paediatrics|September 4, 2010

Associations of progesterone receptor polymorphisms with age at menarche and menstrual cycle lengthK C Taylor, C M Small, M P Epstein, et al.

Nature Genetics|November 1, 1992

Human genes containing polymorphic trinucleotide repeatsG J Riggins, L K Lokey, J L Chastain, et al.

Journal of Medical Genetics|February 1, 2008

Detection of early FXTAS motor symptoms using the CATSYS computerised neuromotor test batteryE G Allen, J Juncos, R Letz, et al.

Human Molecular Genetics|September 1, 1995

Candidate regions for a testicular cancer susceptibility geneM G Leahy, S Tonks, J H Moses, et al.

Human Molecular Genetics|September 1, 1994

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombinationS L Sherman, M B Petersen, S B Freeman, et al.

Clinical Genetics|August 1, 1986

Segregation analysis of balanced pericentric inversions in pedigree dataS L Sherman, L Iselius, P Gallano, et al.

Human Heredity|May 1, 1993

Methodological issues in linkage analyses for psychiatric disorders: secular trends, assortative mating, bilineal pedigrees. Report of the MacArthur Foundation Network I Task Force on Methodological IssuesM A Spence, D T Bishop, M Boehnke, et al.

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