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Clinical Dysmorphology|October 15, 2021
Biallelic DNAJC3 variants in a neuroendocrine developmental disorder with insulin dysregulationSharon Ocansey, Debbie Pullen, Patricia Atkinson, et al.Clinical Dysmorphology|June 5, 2019
Further phenotypic characterization of Kaufman oculocerebrofacial syndrome: report of five new cases and literature reviewCarolina I Galarreta, Kristen M Wigby, Marilyn C JonesClinical Dysmorphology|December 10, 2009
A new case of MOMO syndromeRobert Wallerstein, Rachel D SugalskiClinical Dysmorphology|July 6, 2019
Expansion of phenotype of DDX3X syndrome: six new casesBryony Beal, Ian Hayes, Julie McGaughran, et al.Clinical Dysmorphology|April 24, 2018
A study of familial Char syndrome involving the TFAP2B gene with a focus on facial shape characteristicsDaniel Nyboe, Sven Kreiborg, Tron Darvann, et al.Clinical Dysmorphology|September 13, 2012
Negative mutation screening of the NOG, BMPR1B, GDF5, and FGF9 genes indicates further genetic heterogeneity of the facioaudiosymphalangism syndromeJenneke J van den Ende, Vere Borra, Wim Van HulClinical Dysmorphology|August 5, 1998
Frontonasal dysplasia with optic disc anomalies and other midline craniofacial defects: a report of six casesM M Lees, P Hodgkins, W Reardon, et al.Clinical Dysmorphology|August 5, 1998
Trisomy 9 in an embryo with spina bifidaM J Seller, A Bergbaum, M G DakerClinical Dysmorphology|August 5, 1998
Branchio-oculo-facial syndrome associated with a white forelockA Mégarbané, N Hawat, P Chedid, et al.Clinical Dysmorphology|January 29, 2015
Two cases of Temple-Baraitser syndrome: natural history and further delineation of the clinical and radiologic phenotypesJoseph J ShenPageof 117