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Clinical Genetics|January 11, 1976
Essential tremor, nystagmus and duodenal ulceration. A "new" dominantly inherited conditionG Neuhäuser, R F Daly, N C Magnelli, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXI B: nosologic studies in the Hanhart and the Möbius syndromeJ Herrmann, P D Pallister, E F Gilbert, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1983
Nonsalt-losing congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency with normal glomerulosa functionS Pang, L S Levine, E Stoner, et al.
American Journal of Medical Genetics|June 1, 1982
Studies of malformation syndromes of humans XXXIIIC: the FG syndrome - further studies on three affected individuals from the FG familyJ M Opitz, E G Kaveggia, W N Adkins, et al.
Journal of Medical Genetics|July 11, 2006
The cardiofaciocutaneous syndromeA Roberts, J Allanson, S K Jadico, et al.
American Journal of Medical Genetics|November 1, 1986
New multiple congenital anomalies/mental retardation syndrome with cardio-facio-cutaneous involvement--the CFC syndromeJ F Reynolds, G Neri, J P Herrmann, et al.
American Journal of Medical Genetics. Supplement|January 1, 1987
The Montana Fetal Genetic Pathology Program and a review of prenatal death in humansJ M Opitz, J M FitzGerald, J F Reynolds, et al.
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