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Clinical Genetics|July 1, 1997
Interstitial deletion 2(p11.2p13): a rare chromosomal abnormalityS L Wenger, E W McPhersonCancer Genetics and Cytogenetics|November 1, 1995
Chemical induction of sister chromatid exchange at fragile sitesS L WengerAmerican Journal of Medical Genetics|January 1, 1981
The King syndrome: malignant hyperthermia, myopathy, and multiple anomaliesE W McPherson, C A TaylorAmerican Journal of Medical Genetics|April 1, 1992
Failure of PHA-stimulated i(12p) lymphocytes to divide in Pallister-Killian syndromeS L Reeser, S L WengerCancer Genetics and Cytogenetics|July 1, 1988
Chromosome breaks and fragile sites in leukemic bone marrow cellsK A Przylepa, S L WengerAmerican Journal of Medical Genetics|January 1, 1981
Meiotic consequences of pericentric inversions of chromosome 13S L Wenger, M W SteeleAmerican Journal of Medical Genetics|December 10, 1999
Detection of pericentric inversion of X chromosome in a male fetusS L Wenger, C Cutenese, L R BrancazioCancer Genetics and Cytogenetics|August 1, 1992
Sister chromatid exchange and chromosome breakage in complete hydatidiform molesR A Becker, U Surti, S L WengerGenetic Testing|January 1, 1997
Diagnosis of ataxia telangiectasia with the glycophorin A somatic mutation assayS G Grant, W Reeger, S L WengerAmerican Journal of Medical Genetics|August 15, 1993
Pallister-Killian and Fryns syndromes: nosologyE W McPherson, D M Ketterer, D J SalsbureyPageof 7