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Clinical Dysmorphology|November 19, 2010
Cutaneous features in 17q21.31 deletion syndrome: a differential diagnosis for cardio-facio-cutaneous syndromeEmma Burkitt Wright, Dian Donnai, Diana Johnson, et al.Clinical Dysmorphology|October 1, 1995
Family studies in chromosome 22q11 deletion: further demonstration of phenotypic heterogeneityD De Silva, P Duffty, P Booth, et al.Clinical Dysmorphology|October 1, 1995
Multiple lateral meningoceles, distinctive facies and skeletal anomalies: a new case of Lehman syndromeN Philip, L Andrac, A Moncla, et al.Clinical Dysmorphology|October 1, 1995
Fryns syndrome: two further cases without lateral diaphragmatic defectsO Bartsch, P Meinecke, G KaminClinical Dysmorphology|April 1, 1996
Serpentine fibula syndrome: expansion of the phenotype with three affected siblingsE M Rosser, N P Mann, C M Hall, et al.Clinical Dysmorphology|April 1, 1996
Schinzel-Giedion syndrome: further delineation of the phenotypeA M Elliott, K Meagher-Villemure, K Oudjhane, et al.Clinical Dysmorphology|April 1, 1996
Polysyndactyly and trigonocephaly with partial agenesis of corpus callosumV Guzzetta, M Lecora, G Rossi, et al.Clinical Dysmorphology|January 1, 1996
A neuropsychiatric disorder associated with dense calcification of the external ears and distal muscle wasting: 'Primrose syndrome'N M Lindor, A D Hoffman, D A PrimroseClinical Dysmorphology|January 1, 1996
A second case of microcephaly, microphthalmia, ectrodactyly (split-foot) and prognathism (MMEP)G Suthers, L MorrisClinical Dysmorphology|January 1, 1996
Anterior encephalocele and anophthalmiaL I Al-Gazali, W A Al-ShatherPageof 117