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American Journal of Medical Genetics|May 1, 1988
Investigation of the segregation of the fragile X mutation in daughters of obligate carrier womenS L Sherman, G Turner, H Robinson, et al.American Journal of Human Genetics|November 13, 2001
Multipoint genetic mapping with trisomy dataJ Li, S L Sherman, N Lamb, et al.Clinical Genetics|January 12, 2010
Co-occurring diagnoses among FMR1 premutation allele carriersJ E Hunter, J K Rohr, S L ShermanMelanoma Research|August 1, 1994
Family studies in melanoma: identification of the atypical mole syndrome (AMS) phenotypeJ A Newton Bishop, V Bataille, E Pinney, et al.Molecular Pathology : MP|June 5, 2003
Molecular changes in the Ki-ras and APC genes in primary colorectal carcinoma and synchronous metastases compared with the findings in accompanying adenomasP Zauber, M Sabbath-Solitare, S P Marotta, et al.British Journal of Cancer|January 1, 1997
Germline BRCA2 mutations in men with breast cancerE Mavraki, I C Gray, D T Bishop, et al.American Journal of Human Genetics|April 1, 1993
Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage ConsortiumD F Easton, D T Bishop, D Ford, et al.Neuroscience Letters|July 12, 2011
Cortical fMRI activation to opponents' body kinematics in sport-related anticipation: expert-novice differences with normal and point-light videoM J Wright, D T Bishop, R C Jackson, et al.Scandinavian Journal of Medicine & Science in Sports|November 5, 2015
The influence of motivation and attentional style on affective, cognitive, and behavioral outcomes of an exercise classL Jones, C I Karageorghis, A M Lane, et al.American Journal of Human Genetics|January 1, 1995
Normal variation at the myotonic dystrophy locus in global human populationsC Zerylnick, A Torroni, S L Sherman, et al.Pageof 23