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Clinical Genetics|October 1, 1986
Effect of sibship position on reproductive behavior of couples after the birth of a genetically handicapped childM W Steele, L Rosser, J B Rodnan, et al.American Journal of Medical Genetics|March 13, 1995
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocationJ A Scott, S L Wenger, M W Steele, et al.Pediatric Radiology|January 1, 1984
Multiple exostotic hypochondroplasia: syndrome of combined hypochondroplasia and multiple exostosesR Dominguez, L W Young, M W Steele, et al.Clinical Genetics|August 1, 1984
Prader-Willi syndrome in black femalesW L Golden, J M Hanchett, N Breslin, et al.Annales De Genetique|January 1, 1994
Cytogenetic characterization of cat eye syndrome marker chromosomeS L Wenger, U Surti, N A Nwokoro, et al.Clinical Genetics|January 1, 1984
The level of 6-phosphogluconate dehydrogenase (6-PGD) activity in a patient with 1p terminal deletion suggests that the gene locus is not distal to sub-band p36.3 on chromosome 1M W Steele, S L Wenger, L O Geweke, 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.Pageof 66