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American Journal of Medical Genetics|July 1, 1985
Chondrodysplasia punctata in an infant with duplication 16p due to a 7;16 translocationA G Hunter, D L Rimoin, U M Koch, et al.
The Journal of Biological Chemistry|November 5, 1992
An amino acid substitution (Gly853-->Glu) in the collagen alpha 1(II) chain produces hypochondrogenesisR Bogaert, G E Tiller, M A Weis, et al.
The Journal of Pediatrics|August 1, 1990
Geleophysic dysplasia: a storage disorder affecting the skin, bone, liver, heart, and tracheaM Shohat, H E Gruber, R A Pagon, et al.
Metabolism: Clinical and Experimental|May 1, 1983
A search for heterogeneity in insulin dependent diabetes mellitus (IDDM): HLA and autoimmune studies in simplex, multiplex and multigenerational familiesC E Anderson, S E Hodge, R Rubin, et al.
American Journal of Medical Genetics|October 1, 1990
Rearrangement of chromosome 15 in the region q11.2----q12 in an individual with obesity syndrome and her normal motherM Shohat, T Shohat, D L Rimoin, et al.
Medical and Pediatric Oncology|January 1, 1982
Hodgkin's disease and non-Hodgkin's lymphoma in children and young adults: a clinicopathologic study of 127 casesC Padmalatha, D J Ganick, G R Hafez, et al.
Teratology|August 1, 1978
Aortic aneurysm associated with cardiac defects in theophyline stimulated chick embryosS Ishikawa, E F Gilbert, H J Bruyere, et al.
Archives of Pathology & Laboratory Medicine|April 1, 1981
Islet cell adenomatosis: a report of two cases and review of the literatureR V Lloyd, V Caceres, T F Warner, et al.
Teratology|August 1, 1987
Cardiovascular malformations induced by bromodeoxyuridine in the chick embryoM Nishibatake, S A Kargas, H J Bruyere, et al.
American Journal of Medical Genetics|April 1, 1983
Congenital heart anomalies in the trisomy 18 syndrome, with reference to congenital polyvalvular diseaseR Matsuoka, K Misugi, A Goto, et al.
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