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S L Sherman

Showing results (61-70 of 109) with videos related to

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American Journal of Medical Genetics|August 9, 1996
Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs populationK L Meadows, D Pettay, J Newman, et al.
American Journal of Human Genetics|September 1, 1988
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequenciesC E Aston, S L Sherman, N E Morton, et al.
American Journal of Human Genetics|June 1, 1988
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiencyS L Sherman, C E Aston, N E Morton, et al.
Genetic Epidemiology|January 1, 1997
Sequential sib-pair and association studies to detect genes in quantitative traitsA Savage, F Sun, D C Crawford, et al.
Human Reproduction (Oxford, England)|March 4, 2008
Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary studyJ Rohr, E G Allen, K Charen, et al.
Human Genetics|September 27, 2015
Association between telomere length and chromosome 21 nondisjunction in the oocyteI Albizua, B L Rambo-Martin, E G Allen, et al.
Genes, Chromosomes & Cancer|February 1, 1994
CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosomeG J Riggins, S L Sherman, C N Phillips, et al.
Annals of Neurology|June 1, 1992
Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysisS G Ryan, S L Sherman, J C Terry, et al.
Progress in Clinical and Biological Research|January 1, 1991
Laboratory aspects of prenatal fra(X) detectionE C Jenkins, M S Krawczun, S E Brooks, et al.
Hospitals|August 16, 1985
Health promotion programs flourishing: surveyC K Ross, S L Sherman, K L Berg, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|August 9, 1996
Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs populationK L Meadows, D Pettay, J Newman, et al.
American Journal of Human Genetics|September 1, 1988
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequenciesC E Aston, S L Sherman, N E Morton, et al.
American Journal of Human Genetics|June 1, 1988
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiencyS L Sherman, C E Aston, N E Morton, et al.
Genetic Epidemiology|January 1, 1997
Sequential sib-pair and association studies to detect genes in quantitative traitsA Savage, F Sun, D C Crawford, et al.
Human Reproduction (Oxford, England)|March 4, 2008
Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary studyJ Rohr, E G Allen, K Charen, et al.
Human Genetics|September 27, 2015
Association between telomere length and chromosome 21 nondisjunction in the oocyteI Albizua, B L Rambo-Martin, E G Allen, et al.
Genes, Chromosomes & Cancer|February 1, 1994
CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosomeG J Riggins, S L Sherman, C N Phillips, et al.
Annals of Neurology|June 1, 1992
Startle disease, or hyperekplexia: response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysisS G Ryan, S L Sherman, J C Terry, et al.
Progress in Clinical and Biological Research|January 1, 1991
Laboratory aspects of prenatal fra(X) detectionE C Jenkins, M S Krawczun, S E Brooks, et al.
Hospitals|August 16, 1985
Health promotion programs flourishing: surveyC K Ross, S L Sherman, K L Berg, et al.
Pageof 11