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Showing results (41-50 of 62) with videos related to

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Human Genetics|May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22A R Afzal, A Rajab, C Fenske, et al.
American Journal of Human Genetics|April 1, 1993
Linkage analysis of early-onset breast and ovarian cancer families, with markers on the long arm of chromosome 17N K Spurr, D P Kelsell, D M Black, et al.
Journal of Vascular Surgery|October 1, 1987
Local thrombolysis in peripheral arteries and bypass graftsJ M Pernes, M de Almeida Augusto, J F Vitoux, et al.
Journal of Medical Genetics|February 24, 2001
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 MbR Bell, G Brice, A H Child, et al.
Nature|August 13, 1987
Localization of the gene for familial adenomatous polyposis on chromosome 5W F Bodmer, C J Bailey, J Bodmer, et al.
Princess Takamatsu Symposia|January 1, 1989
Genetic analysis of colorectal cancerW F Bodmer, S Cottrell, A M Frischauf, et al.
Circulation|June 4, 1998
Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21A S Coonar, N Protonotarios, A Tsatsopoulou, et al.
Journal of Medical Genetics|July 13, 2002
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24G Brice, S Mansour, R Bell, et al.
Nature Genetics|August 10, 2000
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2A R Afzal, A Rajab, C D Fenske, et al.
The Journal of Clinical Endocrinology and Metabolism|September 23, 2011
Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effectPhey M Yeap, Edward S Tobias, Eleni Mavraki, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Human Genetics|May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22A R Afzal, A Rajab, C Fenske, et al.
American Journal of Human Genetics|April 1, 1993
Linkage analysis of early-onset breast and ovarian cancer families, with markers on the long arm of chromosome 17N K Spurr, D P Kelsell, D M Black, et al.
Journal of Vascular Surgery|October 1, 1987
Local thrombolysis in peripheral arteries and bypass graftsJ M Pernes, M de Almeida Augusto, J F Vitoux, et al.
Journal of Medical Genetics|February 24, 2001
Reduction of the genetic interval for lyphoedema-distichiasis to below 2 MbR Bell, G Brice, A H Child, et al.
Nature|August 13, 1987
Localization of the gene for familial adenomatous polyposis on chromosome 5W F Bodmer, C J Bailey, J Bodmer, et al.
Princess Takamatsu Symposia|January 1, 1989
Genetic analysis of colorectal cancerW F Bodmer, S Cottrell, A M Frischauf, et al.
Circulation|June 4, 1998
Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21A S Coonar, N Protonotarios, A Tsatsopoulou, et al.
Journal of Medical Genetics|July 13, 2002
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24G Brice, S Mansour, R Bell, et al.
Nature Genetics|August 10, 2000
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2A R Afzal, A Rajab, C D Fenske, et al.
The Journal of Clinical Endocrinology and Metabolism|September 23, 2011
Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effectPhey M Yeap, Edward S Tobias, Eleni Mavraki, et al.
Pageof 7