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S L Wenger

Showing results (11-20 of 73) with videos related to

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Cancer Genetics and Cytogenetics|March 1, 1988
Fragile sites in leukemic bone marrow cellsK A Przylepa, S L Wenger
American Journal of Medical Genetics|July 17, 1995
Fluorescent in situ hybridization for evaluation of Prader-Willi and Angelman syndromesS L Wenger, J H Cummins
American Journal of Medical Genetics|January 1, 1981
Meiotic consequences of pericentric inversions of chromosome 13S L Wenger, M W Steele
Clinical Genetics|July 1, 1997
Interstitial deletion 2(p11.2p13): a rare chromosomal abnormalityS L Wenger, E W McPherson
Clinical Genetics|March 22, 2001
Three-way unbalanced translocation in a mildly dysmorphic mentally retarded childS L Wenger, C Cutenese, M Hummel
American Journal of Medical Genetics|December 10, 1999
Detection of pericentric inversion of X chromosome in a male fetusS L Wenger, C Cutenese, L R Brancazio
Cancer Genetics and Cytogenetics|August 1, 1992
Sister chromatid exchange and chromosome breakage in complete hydatidiform molesR A Becker, U Surti, S L Wenger
Genetic Testing|January 1, 1997
Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assayS G Grant, W Reeger, S L Wenger
Annales De Genetique|January 1, 1991
Assessment of X bends in patients with atypical X chromosome phenotypesC A Munn, S L Wenger, M W Steele
American Journal of Medical Genetics|April 1, 1987
Increased sister chromatid exchange frequency at Xq27 site in affected fragile X malesS L Wenger, J C Hennessey, M W Steele
Pageof 8

Showing results (11-20 of 73) with videos related to

Sort By:
Pageof 8
Cancer Genetics and Cytogenetics|March 1, 1988
Fragile sites in leukemic bone marrow cellsK A Przylepa, S L Wenger
American Journal of Medical Genetics|July 17, 1995
Fluorescent in situ hybridization for evaluation of Prader-Willi and Angelman syndromesS L Wenger, J H Cummins
American Journal of Medical Genetics|January 1, 1981
Meiotic consequences of pericentric inversions of chromosome 13S L Wenger, M W Steele
Clinical Genetics|July 1, 1997
Interstitial deletion 2(p11.2p13): a rare chromosomal abnormalityS L Wenger, E W McPherson
Clinical Genetics|March 22, 2001
Three-way unbalanced translocation in a mildly dysmorphic mentally retarded childS L Wenger, C Cutenese, M Hummel
American Journal of Medical Genetics|December 10, 1999
Detection of pericentric inversion of X chromosome in a male fetusS L Wenger, C Cutenese, L R Brancazio
Cancer Genetics and Cytogenetics|August 1, 1992
Sister chromatid exchange and chromosome breakage in complete hydatidiform molesR A Becker, U Surti, S L Wenger
Genetic Testing|January 1, 1997
Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assayS G Grant, W Reeger, S L Wenger
Annales De Genetique|January 1, 1991
Assessment of X bends in patients with atypical X chromosome phenotypesC A Munn, S L Wenger, M W Steele
American Journal of Medical Genetics|April 1, 1987
Increased sister chromatid exchange frequency at Xq27 site in affected fragile X malesS L Wenger, J C Hennessey, M W Steele
Pageof 8