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Clinical Dysmorphology|August 25, 2022
De novo interstitial deletion of 11q14.3q22 in a boy with mild intellectual disability and short statureFatma Kurt Colak, Nilnur Eyerci, Naz Guleray LafciClinical Dysmorphology|August 5, 1998
Variable phenotype in Kaufman-McKusick syndrome: report of an inbred Muslim family and review of the literatureD Kumar, R A Primhak, A KumarClinical Dysmorphology|August 5, 1998
Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearanceL I al-Gazali, D BakalinovaClinical Dysmorphology|August 5, 1998
Variability of platyspondylic lethal chondrodysplasia: another case reportG Nishimura, T Iwasawa, R Fukuzawa, et al.Clinical Dysmorphology|August 17, 2012
VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysisEnrika Bartels, Anna C Schulz, Nicole W Mora, et al.Clinical Dysmorphology|May 7, 2004
Dysmorphic facial features in aspartylglucosaminuria patients and carriersMaria A Arvio, Maarit M Peippo, Pekka J Arvio, et al.Clinical Dysmorphology|May 7, 2004
Axial mesodermal dysplasia sequence: autopsy findingsSaumil N Merchant, Timothy S Naimi, Aayesha Khan, et al.Clinical Dysmorphology|May 7, 2004
Loose anagen hair syndrome associated with colobomas and dysmorphic featuresLars Kjaersgård Hansen, Flemming Brandrup, Ole ClemmensenClinical Dysmorphology|May 7, 2004
Seckel syndrome associated with atrioventricular canal defect: a case reportBirsen Ucar, Zübeyir Kilic, Ener Cagri Dinleyici, et al.Clinical Dysmorphology|September 13, 2005
Duplication of the Down syndrome critical region does not predict facial phenotype in a baby with a ring chromosome 21Eric A Crombez, Katrina M Dipple, Lisa A Schimmenti, et al.Pageof 117