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S L Sherman

Showing results (31-40 of 109) with videos related to

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Human 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 Dobkin
Annals 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 Sherman
Annals of Human Genetics|July 1, 1985
A genetic map of chromosome 19 based on family linkage dataS L Sherman, S P Ball, E B Robson
Cytogenetic 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 Hassold
American 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 Ashley
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 Sherman
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.
Genetic Epidemiology|January 1, 1995
Identification of susceptibility loci contributing to a complex disease using conventional segregation, linkage, and association methodsC T Falk, A Ashley, N Lamb, et al.
Pageof 11

Showing results (31-40 of 109) with videos related to

Sort By:
Pageof 11
Human 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 Dobkin
Annals 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 Sherman
Annals of Human Genetics|July 1, 1985
A genetic map of chromosome 19 based on family linkage dataS L Sherman, S P Ball, E B Robson
Cytogenetic 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 Hassold
American 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 Ashley
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 Sherman
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.
Genetic Epidemiology|January 1, 1995
Identification of susceptibility loci contributing to a complex disease using conventional segregation, linkage, and association methodsC T Falk, A Ashley, N Lamb, et al.
Pageof 11