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Clinical Dysmorphology|December 1, 2007
Three siblings with Woodhouse-Sakati syndrome in an Indian familyGeorge Koshy, Sumita Danda, Nihal Thomas, et al.Clinical Dysmorphology|March 15, 2006
Two female siblings with congenital heart disease, postaxial polydactyly, ectopic neuropituitary gland, hair anomalies and characteristic facial features: a new syndrome?Linde Goossens, Sandra Janssens, Valerie Meersschaut, et al.Clinical Dysmorphology|March 15, 2006
Monosomy 5p and trisomy 12p in a boy with familial balanced translocationPradeep C Vasudevan, Michael J ParkerClinical Dysmorphology|March 15, 2006
A case of Beare-Stevenson syndrome with a broad spectrum of features and a review of the FGFR2 Y375C mutation phenotypeJulie McGaughran, Stephen Sinnott, Rachel Susman, et al.Clinical Dysmorphology|March 15, 2006
Microcephaly, lissencephaly, Hirschsprung disease and tetralogy of Fallot: a new syndrome?George A Tanteles, Beena Kurup, Anita Rauch, et al.Clinical Dysmorphology|March 15, 2006
Visual impairment and prolonged survival in a girl with Marshall-Smith syndromeCharulata Deshpande, Michael Forrest, Isabelle Russell-Eggitt, et al.Clinical Dysmorphology|March 15, 2006
Multiple renal cysts, ear anomalies, disordered hair growth and unusual facies: a new entity?Emma McCann, Elizabeth Sweeney, Janette DalyClinical Dysmorphology|October 21, 2016
De-novo 'pure' partial trisomy (6)(p22.3→pter): a case report and review of the literatureAswini Sivasankaran, Kanakavalli Murthy, Venkata P Oruganti, et al.Clinical Dysmorphology|March 13, 2014
Variable clinical presentation in primary lymphoedema: report of two casesAbdullah Ozyurt, Eylem Sevinc, Ali Baykan, et al.Clinical Dysmorphology|April 7, 2017
A novel case of autosomal dominant cutis laxa in a consanguineous family: report and literature reviewMehmet B Duz, Emre Kirat, Paul J Coucke, et al.Pageof 117