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S L Sherman

Showing results (21-30 of 109) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1990
Report of the committee on linkage and gene orderB J Keats, S L Sherman, J Ott
Cytogenetics and Cell Genetics|January 1, 1985
Report of the Committee on the Genetic Constitution of Chromosomes 1 and 2S Povey, N E Morton, S L Sherman
American Journal of Human Genetics|March 11, 2000
Multipoint estimation of genetic maps for human trisomies with one parent or other partial dataE Feingold, A S Brown, S L Sherman
Human Molecular Genetics|November 25, 2000
Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCRD C Crawford, B Wilson, S L Sherman
American Journal of Human Genetics|February 1, 1995
Methods for genetic linkage analysis using trisomiesE Feingold, N E Lamb, S L Sherman
Genomics|June 1, 1993
Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage mapS Todd, S L Sherman, S L Naylor
Genetics|July 1, 1997
Estimating meiotic exchange patterns from recombination data: an application to humansN E Lamb, E Feingold, S L Sherman
Biochemical Society Transactions|July 22, 2006
Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21S L Sherman, N E Lamb, E Feingold
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 Sherman
Chromosoma|June 26, 1998
Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndromeJ J Shen, S L Sherman, T J Hassold
Pageof 11

Showing results (21-30 of 109) with videos related to

Sort By:
Pageof 11
Cytogenetics and Cell Genetics|January 1, 1990
Report of the committee on linkage and gene orderB J Keats, S L Sherman, J Ott
Cytogenetics and Cell Genetics|January 1, 1985
Report of the Committee on the Genetic Constitution of Chromosomes 1 and 2S Povey, N E Morton, S L Sherman
American Journal of Human Genetics|March 11, 2000
Multipoint estimation of genetic maps for human trisomies with one parent or other partial dataE Feingold, A S Brown, S L Sherman
Human Molecular Genetics|November 25, 2000
Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCRD C Crawford, B Wilson, S L Sherman
American Journal of Human Genetics|February 1, 1995
Methods for genetic linkage analysis using trisomiesE Feingold, N E Lamb, S L Sherman
Genomics|June 1, 1993
Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage mapS Todd, S L Sherman, S L Naylor
Genetics|July 1, 1997
Estimating meiotic exchange patterns from recombination data: an application to humansN E Lamb, E Feingold, S L Sherman
Biochemical Society Transactions|July 22, 2006
Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21S L Sherman, N E Lamb, E Feingold
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 Sherman
Chromosoma|June 26, 1998
Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndromeJ J Shen, S L Sherman, T J Hassold
Pageof 11