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S L Sherman

Showing results (41-50 of 109) with videos related to

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Annals of Human Genetics|July 1, 1984
A revised map of chromosome 1S L Sherman, J King, E B Robson, et al.
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|May 1, 1988
The longitudinal effects of growth on the Wits appraisalS L Sherman, M Woods, R S Nanda, et al.
Human Molecular Genetics|March 4, 2000
Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21A S Brown, E Feingold, K W Broman, et al.
American Journal of Medical Genetics|May 1, 1988
Investigation of the twinning rate in families with the fragile X syndromeS L Sherman, G Turner, L Sheffield, et al.
Annals of Human Genetics|January 1, 1984
The marker (X) syndrome: a cytogenetic and genetic analysisS L Sherman, N E Morton, P A Jacobs, et al.
Genetic Epidemiology. Supplement|January 1, 1986
Combined segregation and linkage analysis of multiple sclerosisS L Sherman, R W Haile, C J MacLean, et al.
Cytogenetic and Genome Research|September 30, 2005
Risk factors for nondisjunction of trisomy 21S L Sherman, S B Freeman, E G Allen, et al.
Cytogenetics and Cell Genetics|January 1, 1992
An application of empirical Bayes methods to updating linkage information on chromosome 21G E Bonney, K K Amfoh, S L Sherman, et al.
Genetic Epidemiology|January 1, 1984
Genetic Analysis Workshop II: combined segregation, linkage, and association analysisN E Morton, S L Sherman, S MacLean, et al.
American Journal of Human Genetics|February 1, 1993
Distribution of lod scores under uncertain mode of inheritanceC J MacLean, D T Bishop, S L Sherman, et al.
Pageof 11

Showing results (41-50 of 109) with videos related to

Sort By:
Pageof 11
Annals of Human Genetics|July 1, 1984
A revised map of chromosome 1S L Sherman, J King, E B Robson, et al.
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|May 1, 1988
The longitudinal effects of growth on the Wits appraisalS L Sherman, M Woods, R S Nanda, et al.
Human Molecular Genetics|March 4, 2000
Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21A S Brown, E Feingold, K W Broman, et al.
American Journal of Medical Genetics|May 1, 1988
Investigation of the twinning rate in families with the fragile X syndromeS L Sherman, G Turner, L Sheffield, et al.
Annals of Human Genetics|January 1, 1984
The marker (X) syndrome: a cytogenetic and genetic analysisS L Sherman, N E Morton, P A Jacobs, et al.
Genetic Epidemiology. Supplement|January 1, 1986
Combined segregation and linkage analysis of multiple sclerosisS L Sherman, R W Haile, C J MacLean, et al.
Cytogenetic and Genome Research|September 30, 2005
Risk factors for nondisjunction of trisomy 21S L Sherman, S B Freeman, E G Allen, et al.
Cytogenetics and Cell Genetics|January 1, 1992
An application of empirical Bayes methods to updating linkage information on chromosome 21G E Bonney, K K Amfoh, S L Sherman, et al.
Genetic Epidemiology|January 1, 1984
Genetic Analysis Workshop II: combined segregation, linkage, and association analysisN E Morton, S L Sherman, S MacLean, et al.
American Journal of Human Genetics|February 1, 1993
Distribution of lod scores under uncertain mode of inheritanceC J MacLean, D T Bishop, S L Sherman, et al.
Pageof 11