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Epilepsia|March 1, 1989
Lack of sister chromatid exchange induction in phenytoin-treated patients with epilepsyB A Schaumann, V B Winge, V F GarryEpilepsy Research|March 1, 1989
Sister chromatid exchanges in adult epilepsy patients on valproate monotherapyB A Schaumann, V B Winge, V F GarryPostgraduate Medicine|January 1, 1979
Syndrome delineation. 1. Malformations and dysplasiasJ Herrmann, J M OpitzEuropean Journal of Pediatrics|June 1, 1977
The SC phocomelia and the Roberts syndrome: nosologic aspectsJ Herrmann, J M OpitzClinical Genetics|May 1, 1975
Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadismG Neuhäuser, J M OpitzAmerican Journal of Medical Genetics|July 27, 2001
Comments on biological asymmetryJ M Opitz, A UtkusAmerican Journal of Medical Genetics|January 1, 1977
Pericentric inversion of chromosome 14 and the risk of partial duplication of 14q (14q31 leads to 14qter)C Trunca, J M OpitzZeitschrift Fur Kinderheilkunde|November 13, 1975
Studies of malformation syndromes in man XXXX: multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father)G Neuhäuser, J M OpitzPostgraduate Medicine|February 1, 1979
Syndrome delineation. 2. Inborn errors of metabolism, deformities, and variant familial developmental patternsJ Herrmann, J M OpitzAmerican Journal of Medical Genetics|July 14, 2001
Sixty years of X-linked mental retardation: a historical footnoteG Neri, J M OpitzPageof 19