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Clinical Genetics|May 1, 1987
The Angelman (Happy Puppet) syndrome: is it autosomal recessive?M Baraitser, M Patton, S T Lam, et al.Journal of Medical Genetics|January 1, 1990
De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomaliesI K Temple, J A Hurst, S Hing, et al.Prenatal Diagnosis|March 1, 1986
Prenatal treatment of fetal hydrops associated with the hypertelorism-dysphagia syndrome (Opitz-G syndrome)M A Patton, M Baraitser, K Nickolaides, et al.Brain : a Journal of Neurology|June 1, 1980
The incidence and nature of visual pathway involvement in Friedreich's ataxia. A clinical and visual evoked potential study of 22 patientsW M Carroll, A Kriss, M Baraitser, et al.Clinical Dysmorphology|July 1, 1996
Nance-Sweeney chondrodysplasia--a further case?E M Rosser, C M Hall, J Harper, et al.Clinical Genetics|November 1, 1990
Partial lipodystrophy syndromes--a further male caseW Reardon, I K Temple, H Mackinnon, et al.Neuropediatrics|February 1, 1992
Autosomal recessive microcephaly with severe psychomotor retardationI E Scheffer, M Baraitser, J Wilson, et al.Journal of Medical Genetics|September 1, 1995
Monozygotic twins with chromosome 22q11 deletion and discordant phenotypeJ Goodship, I Cross, P Scambler, et al.Journal of Medical Genetics|June 1, 1994
Meckel syndrome: what are the minimum diagnostic criteria?C Wright, R Healicon, C English, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2016
Orthostatic hypotension and cognitive impairment in Parkinson's disease: Causation or association?Claire McDonald, Julia L Newton, David J BurnPageof 60