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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.Sheng Wu Yi Xue Gong Cheng Xue Za Zhi = Journal of Biomedical Engineering = Shengwu Yixue Gongchengxue Zazhi|January 29, 2003
[The test of mean flow velocity patterns within a new push-plate ventricular assist device]S PanThe Journal of Pediatrics|October 1, 1996
A simplified six-item checklist for screening for fragile X syndrome in the pediatric populationC A Giangreco, M W Steele, C E Aston, et al.American Journal of Medical Genetics|October 1, 1992
Acrometageria: a spectrum of "premature aging" syndromesJ M Greally, L Y Boone, S G Lenkey, et al.American Journal of Medical Genetics|August 1, 1992
X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriersS L Wenger, M W Steele, E P Hoffman, et al.American Journal of Medical Genetics|December 1, 1987
Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletionS L Wenger, J M Hanchett, M W Steele, et al.Pageof 66