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Prenatal Diagnosis|April 1, 1994
Prenatal diagnosis and dysmorphic findings in mosaic trisomy 16A Garber, D Carlson, R Schreck, et al.
American Journal of Medical Genetics|June 9, 1999
Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluationL G Biesecker, R Happle, J B Mulliken, et al.
Prenatal Diagnosis|October 1, 1993
Preaxial ray reduction defects as part of valproic acid embryofetopathyR Sharony, A Garber, D Viskochil, et al.
The Journal of Clinical Investigation|October 1, 1989
Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotypeB J Starman, D Eyre, H Charbonneau, et al.
American Journal of Medical Genetics|December 25, 1991
Radiological findings in Hallermann-Streiff syndrome: report of five cases and a review of the literatureC L Christian, R S Lachman, A S Aylsworth, et al.
Behavioural Brain Research|January 1, 1982
Analysis of facial displays and verbal report to assess subjective state in the non-invasive detection of limbic system activation by procaine hydrochlorideC Stark-Adamec, R E Adamec, J M Graham, et al.
American Journal of Medical Genetics|January 1, 1991
Congenital gastric teratoma in Wiedemann-Beckwith syndromeT C Falik-Borenstein, J R Korenberg, I Davos, et al.
American Journal of Medical Genetics|April 11, 1991
Deletion of 20p 11.23----pter with normal growth hormone-releasing hormone genesM Shohat, V Herman, S Melmed, et al.
American Journal of Medical Genetics|November 15, 1993
Congenital diaphragmatic hernia in the Brachmann-de Lange syndromeC Cunniff, C J Curry, J C Carey, et al.
Pharmacogenetics|March 30, 2000
Association study of dopamine receptor gene polymorphisms with drug-induced hallucinations in patients with idiopathic Parkinson's diseaseA J Makoff, J M Graham, M J Arranz, et al.
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