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Clinical Dysmorphology|April 1, 1994
Megalocornea, developmental retardation and dysmorphic features: two further patientsM L Gibbs, A O Wilkie, R M Winter, et al.American Journal of Medical Genetics|October 1, 1983
The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identityR M Winter, M Baraitser, K M Laurence, et al.Journal of Medical Genetics|May 1, 1989
Moore-Federman syndrome and acromicric dysplasia: are they the same entity?R M Winter, M A Patton, J Challener, et al.Journal of Medical Genetics|December 14, 1999
Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32M M Lees, R M Winter, S Malcolm, et al.Clinical Dysmorphology|April 18, 1998
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)J Amiel, P M Watkin, M Tassabehji, et al.Journal of Medical Genetics|June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palateS E Holder, G M Vintiner, B Farren, et al.Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.Human Molecular Genetics|July 1, 1997
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3S A Feather, A S Woolf, D Donnai, et al.Clinical Dysmorphology|January 1, 1993
Previously unrecognized form of familial spondyloepiphyseal dysplasia tarda with characteristic faciesS M Huson, S Crowley, C M Hall, et al.Pageof 19