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The 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.American Journal of Medical Genetics|January 2, 1995
"Balanced" karyotypes in six abnormal offspring of balanced reciprocal translocation normal carrier parentsS L Wenger, M W Steele, L Y Boone, et al.Hormone Research|January 1, 1988
46XY siblings with inadequate virilization and CNS deficiencyR P Hoffman, M W Steele, P A Lee, et al.Proceedings of the National Academy of Sciences of the United States of America|October 15, 1991
X/Y translocations resulting from recombination between homologous sequences on Xp and YqP H Yen, S P Tsai, S L Wenger, et al.Cancer Genetics and Cytogenetics|April 1, 1988
Rhabdomyosarcoma in Roberts syndromeS L Wenger, J Blatt, M W Steele, et al.American Journal of Medical Genetics|February 15, 1994
Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypesA M Estop, V Bansal, A Lin, et al.American Journal of Medical Genetics|November 1, 1988
Interstitial and terminal deletions of the long arm of chromosome 4: further delineation of phenotypesA E Lin, K L Garver, G Diggans, et al.Pageof 5