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Clinical Genetics|May 1, 1976
Trisomy of chromosome 20S F Pan, S R Fatora, J E Haas, et al.
American Journal of Medical Genetics|January 1, 1990
Chromosome mosaicism in hypomelanosis of ItoC L Ritter, M W Steele, S L Wenger, et al.
American Journal of Medical Genetics|May 16, 1997
Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromesS L Wenger, S L Sell, M J Painter, et al.
Clinical Genetics|July 1, 1986
Relative reliability of three different discriminant analysis methods for detecting PKU gene carriersS L Wenger, P W Vieira, J M Breck, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|May 1, 1989
The fragile X marker and autism in perspectiveJ B Payton, M W Steele, S L Wenger, et al.
American Journal of Medical Genetics|February 27, 1995
Chromosomal abnormalities in a psychiatric populationK E Lewis, M J Lubetsky, S L Wenger, et al.
Ophthalmic Paediatrics and Genetics|March 1, 1993
Broad-spectrum Möbius syndrome associated with a 1;11 chromosome translocationS P Donahue, S L Wenger, M W Steele, et al.
American Journal of Medical Genetics|December 1, 1984
Are the occasional aneuploid cells in peripheral blood cultures significant?S L Wenger, W L Golden, S P Dennis, et al.
Clinical Genetics|November 1, 1977
Meiotic consequences of an intrachromosomal insertion of chromosome No 1: a family pedigreeS F Pan, S R Fatora, R Sorg, et al.
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