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Clinical Dysmorphology|June 3, 2005
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndromeElisabetta Tabolacci, Marcella Zollino, Rosetta Lecce, et al.Clinical Dysmorphology|June 3, 2005
Blepharocheilodontic syndrome or lagophthalmos: a child with overlapping featuresIngrid Winship, Salim AftimosClinical Dysmorphology|June 3, 2005
Congenital melanocytic naevus with associated neurofibroma and schwannoma-like changeEmma McCann, Alan E Fryer, George KokaiClinical Dysmorphology|June 3, 2005
Caudothalamic groove cysts in Zellweger syndromeBülent Ünay, Tanıl Kendirli, Kaan Atac, et al.Clinical Dysmorphology|December 1, 2007
Phenotypic variation in trismus-pseudocamptodactyly syndrome caused by a recurrent MYH8 mutationKaren Minzer-Conzetti, Erica Wu, Karin Vargervik, et al.Clinical Dysmorphology|December 1, 2007
Screening for subtelomeric chromosome alteration in a consecutive series of newborns with congenital defectsLaura Rodríguez, María Luisa Martínez-Fernández, Elena Mansilla, et al.Clinical Dysmorphology|December 1, 2007
A patient with de-novo partial deletion of Xp (p11.4-pter) and partial duplication of 22q (q11.2-qter)Christine M Armour, Jean McGowan-Jordan, Sarah E Lawrence, et al.Clinical Dysmorphology|December 1, 2007
De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairmentTomoki Kosho, Satoru Sakazume, Hiroshi Kawame, et al.Clinical Dysmorphology|March 15, 2006
Pfeiffer-type cardiocranial syndrome: a patient with features of this condition and with an unbalanced subtelomeric rearrangement involving chromosomes 1p and 17qEmma McCann, Elizabeth Sweeney, John Sills, et al.Clinical Dysmorphology|November 21, 1998
Adams-Oliver syndrome associated with cardiovascular malformationsA E Lin, M N Westgate, M E van der Velde, et al.Pageof 117