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Journal of Child Neurology|August 2, 2000
Diffuse polymicrogyria associated with congenital hydrocephalus, craniosynostosis, severe mental retardation, and minor facial and genital anomaliesL Pavone, R Rizzo, P Pavone, et al.Neuroradiology|October 1, 1996
Congenital pontocerebellar atrophy in three patients: clinical, radiologic and etiologic considerationsN Zelnik, W B Dobyns, S L Forem, et al.Journal of Child Neurology|January 1, 1990
Isolated lissencephaly: report of four patients from two unrelated familiesL Pavone, F Gullotta, G Incorpora, et al.Pediatric Neurology|May 1, 1997
Valproate-induced liver failure in one of two siblings with Alpers diseaseM J Schwabe, W B Dobyns, B Burke, et al.Postgraduate 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 OpitzPageof 40