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S L Sherman

Showing results (51-60 of 109) with videos related to

Pageof 11
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Journal of Medical Genetics|May 5, 2009
Germline mutation of microRNA-125a is associated with breast cancerW Li, R Duan, F Kooy, et al.
Progress in Clinical and Biological Research|January 1, 1989
Mapping strategies for multiple linked markersM C Speer, S L Sherman, C S Haynes, et al.
Genetic Epidemiology. Supplement|January 1, 1986
Combined segregation and linkage analysis of coeliac diseaseS L Sherman, L Iselius, A Ellis, et al.
Human Molecular Genetics|August 1, 2000
Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instabilityD C Crawford, F Zhang, B Wilson, et al.
American Journal of Human Genetics|March 25, 2000
Women with a reduced ovarian complement may have an increased risk for a child with Down syndromeS B Freeman, Q Yang, K Allran, et al.
Genetic Epidemiology|January 1, 1996
Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disordersF Mili, W D Flanders, S L Sherman, et al.
American Journal of Medical Genetics|May 7, 2002
Cognitive and behavioral performance among FMR1 high-repeat allele carriers surveyed from special education classesS L Sherman, F Marsteller, A J Abramowitz, et al.
International Journal of Shoulder Surgery|July 13, 2012
Clinical outcomes of revision biceps tenodesisJ M Gregory, D P Harwood, E Gochanour, et al.
American Journal of Human Genetics|June 4, 2026
Patricia A. Jacobs (1934-2026)S Ennis, S L Sherman, T J Hassold, et al.
American Journal of Human Genetics|August 1, 1991
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal regionT J Hassold, S L Sherman, D Pettay, et al.
Pageof 11

Showing results (51-60 of 109) with videos related to

Sort By:
Pageof 11
Journal of Medical Genetics|May 5, 2009
Germline mutation of microRNA-125a is associated with breast cancerW Li, R Duan, F Kooy, et al.
Progress in Clinical and Biological Research|January 1, 1989
Mapping strategies for multiple linked markersM C Speer, S L Sherman, C S Haynes, et al.
Genetic Epidemiology. Supplement|January 1, 1986
Combined segregation and linkage analysis of coeliac diseaseS L Sherman, L Iselius, A Ellis, et al.
Human Molecular Genetics|August 1, 2000
Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instabilityD C Crawford, F Zhang, B Wilson, et al.
American Journal of Human Genetics|March 25, 2000
Women with a reduced ovarian complement may have an increased risk for a child with Down syndromeS B Freeman, Q Yang, K Allran, et al.
Genetic Epidemiology|January 1, 1996
Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disordersF Mili, W D Flanders, S L Sherman, et al.
American Journal of Medical Genetics|May 7, 2002
Cognitive and behavioral performance among FMR1 high-repeat allele carriers surveyed from special education classesS L Sherman, F Marsteller, A J Abramowitz, et al.
International Journal of Shoulder Surgery|July 13, 2012
Clinical outcomes of revision biceps tenodesisJ M Gregory, D P Harwood, E Gochanour, et al.
American Journal of Human Genetics|June 4, 2026
Patricia A. Jacobs (1934-2026)S Ennis, S L Sherman, T J Hassold, et al.
American Journal of Human Genetics|August 1, 1991
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal regionT J Hassold, S L Sherman, D Pettay, et al.
Pageof 11