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Clinical Dysmorphology|September 6, 2007
Supernumerary nostrils together with oesophageal atresia and patent ductus arteriosusVarim Numanoglu, Bahri Ermis, Ahmet Dursun, et al.Clinical Dysmorphology|September 6, 2007
A patient with Mullerian abnormalities, renal dysplasia, cervical spine fusion, cataracts and intellectual disability: MURCS-plus?Tiong Yang Tan, Charlotte Whitelaw, Ravi SavarirayanClinical Dysmorphology|December 18, 2008
De-novo 2.15 Mb terminal Xq duplication involving MECP2 but not L1CAM gene in a male patient with mental retardationMilen Velinov, Antonio Novelli, Hong Gu, et al.Clinical Dysmorphology|December 6, 2008
Hallerman-Streiff-like syndrome presenting with laterality and cardiac defectsFanny Morice-Picard, Sandrine Marlin, Caroline Rooryck, et al.Clinical Dysmorphology|February 4, 2009
Tetraphocomelia with the Waardenburg syndrome and multiple malformationsHue-Tsi Wu, Helen Wainwright, Peter BeightonClinical Dysmorphology|December 15, 2012
A nonsense mutation in the gene ROR2 underlying autosomal dominant brachydactyly type BRabia Habib, Muhammad Amin-Ud-Din, Wasim AhmadClinical Dysmorphology|April 25, 2013
Genotype-phenotype study in type V osteogenesis imperfectaMeena Balasubramanian, Michael J Parker, Ann Dalton, et al.Clinical Dysmorphology|November 29, 2012
Differences in the clinical spectrum of two adolescent male patients with Alström syndromeVladimir Kuburović, Jan D Marshall, Gayle B Collin, et al.Clinical Dysmorphology|August 24, 2000
A case of the new overgrowth syndrome--macrocephaly with cutis marmorata, haemangioma and syndactylyD Baralle, H FirthClinical Dysmorphology|May 8, 2026
Clinical spectrum of acyl-CoA synthetase family member 3-related combined malonic and methylmalonic aciduria: insights from four casesSabire Gokalp, Hacer Basan, Asburce Olgac, et al.Pageof 117