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P K Rogan

Showing results (41-50 of 45) with videos related to

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American Journal of Human Genetics|July 27, 1999
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpointsJ M Amos-Landgraf, Y Ji, W Gottlieb, et al.
American Journal of Medical Genetics|July 1, 1993
Clinical and molecular analyses of deletion 3p25-pter syndromeP N Mowrey, M J Chorney, C P Venditti, et al.
American Journal of Human Genetics|February 11, 1999
Imprinting-mutation mechanisms in Prader-Willi syndromeT Ohta, T A Gray, P K Rogan, et al.
Breast Cancer Research and Treatment|December 14, 2017
Assessment of the functional impact of germline BRCA1/2 variants located in non-coding regions in families with breast and/or ovarian cancer predispositionE Santana Dos Santos, S M Caputo, L Castera, et al.
American Journal of Medical Genetics|January 20, 1997
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutationS Saitoh, K Buiting, S B Cassidy, et al.
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Showing results (41-50 of 45) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 45 results.
American Journal of Human Genetics|July 27, 1999
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpointsJ M Amos-Landgraf, Y Ji, W Gottlieb, et al.
American Journal of Medical Genetics|July 1, 1993
Clinical and molecular analyses of deletion 3p25-pter syndromeP N Mowrey, M J Chorney, C P Venditti, et al.
American Journal of Human Genetics|February 11, 1999
Imprinting-mutation mechanisms in Prader-Willi syndromeT Ohta, T A Gray, P K Rogan, et al.
Breast Cancer Research and Treatment|December 14, 2017
Assessment of the functional impact of germline BRCA1/2 variants located in non-coding regions in families with breast and/or ovarian cancer predispositionE Santana Dos Santos, S M Caputo, L Castera, et al.
American Journal of Medical Genetics|January 20, 1997
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutationS Saitoh, K Buiting, S B Cassidy, et al.
Pageof 5