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Clinical Dysmorphology|October 18, 2003
An Irish three-generation family of Cornelia de Lange syndrome displaying autosomal dominant inheritanceV McConnell, T Brown, P J MorrisonClinical Dysmorphology|October 18, 2003
Macrocephaly and sclerosis of the tubular bones in an isolated patient: a mild case of craniodiaphyseal dysplasia?Katrien Janssens, Elizabeth Thompson, Filip Vanhoenacker, et al.Clinical Dysmorphology|October 18, 2003
Thyroid hypoplasia of the left lobe in two girls affected by Williams syndromeStefano Stagi, Giuseppe Bindi, Anna Silvia Neri, et al.Clinical Dysmorphology|October 18, 2003
Type 1 Arnold-Chiari malformation and Noonan syndrome. A new diagnostic feature?Muriel Holder-Espinasse, Robin M WinterClinical Dysmorphology|November 4, 2008
Chondrodysplasia punctata: a clinical diagnostic and radiological reviewMelita D Irving, Lyn S Chitty, Sahar Mansour, et al.Clinical Dysmorphology|July 9, 2020
Recurrent c.776T>C mutation in CHST3 with four other novel mutations and a literature reviewMehmet Bugrahan Duz, Ali TopakClinical Dysmorphology|March 28, 2015
An unusual presentation of oculoauriculovertebral spectrum with a Tessier 30 cleft: report on two casesSiulan Vendramini-Pittoli, Maria L Guion-Almeida, Juliana M Santos, et al.Clinical Dysmorphology|February 26, 2015
An interstitial de-novo microdeletion of 3q26.33q27.3 causing severe intrauterine growth retardationArjan Bouman, Marjan Weiss, Sandra Jansen, et al.Clinical Dysmorphology|October 23, 2001
Precocious puberty, endometriosis, skeletal anomalies and mild hearing loss: a new autosomal dominant syndrome?J M McGaughran, D A Price, B A KerrClinical Dysmorphology|February 2, 2002
Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocationAdnan Yuksel, Mehmet Seven, Birsen Karaman, et al.Pageof 117