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Annals of Human Genetics|February 20, 2002
Nonsyndromic cleft lip and palate: complex genetics and environmental effectsN J Prescott, R M Winter, S MalcolmHuman Genetics|May 8, 2000
Identification of susceptibility loci for nonsyndromic cleft lip with or without cleft palate in a two stage genome scan of affected sib-pairsN J Prescott, M M Lees, R M Winter, et al.Human Genetics|October 1, 1986
Gene localisation of X-linked hypohidrotic ectodermal dysplasia (C-S-T syndrome)K D MacDermot, R M Winter, S MalcolmJournal of Medical Genetics|June 1, 1992
No evidence of linkage between the transforming growth factor-alpha gene in families with apparently autosomal dominant inheritance of cleft lip and palateG M Vintiner, S E Holder, R M Winter, et al.American Journal of Human Genetics|October 1, 1992
Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosisS Strautnieks, P Rutland, R M Winter, et al.Human Molecular Genetics|August 1, 1997
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic casesC S Rose, P Patel, W Reardon, 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.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.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.Journal of Medical Genetics|March 1, 1994
Crouzon syndrome is not linked to craniosynostosis loci at 7p and 5qterW Reardon, L van Herwerden, C Rose, et al.Pageof 37