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Genetics|July 1, 1997
Estimating meiotic exchange patterns from recombination data: an application to humansN E Lamb, E Feingold, S L ShermanBiochemical Society Transactions|July 22, 2006
Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21S L Sherman, N E Lamb, E FeingoldHuman Molecular Genetics|December 1, 2001
A deep intronic mutation in CDKN2A is associated with disease in a subset of melanoma pedigreesM Harland, S Mistry, D T Bishop, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2001
FMR1 and the fragile X syndrome: human genome epidemiology reviewD C Crawford, J M Acuña, S L ShermanChromosoma|June 26, 1998
Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndromeJ J Shen, S L Sherman, T J HassoldHuman Genetics|March 1, 1987
Hypothesis regarding the nature of the fragile X mutation. A reply to Winter and PembreyW T Brown, S L Sherman, C S DobkinAnnals of Human Genetics|January 30, 1999
A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutationR M Huggins, D Z Loesch, S L ShermanAnnals of Human Genetics|July 1, 1985
A genetic map of chromosome 19 based on family linkage dataS L Sherman, S P Ball, E B RobsonCytogenetic and Genome Research|September 30, 2005
Effect of meiotic recombination on the production of aneuploid gametes in humansN E Lamb, S L Sherman, T J HassoldAmerican Journal of Medical Genetics|August 9, 1996
Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier femalesS L Sherman, K L Meadows, A E AshleyPageof 23