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Clinical Dysmorphology|January 1, 1992
Fetus with unbalanced translocation involving chromosomes 2 and 11A M Norman, A P Read, A Clark, et al.American Journal of Medical Genetics|February 5, 1998
Choanal atresia and hypothelia following methimazole exposure in utero: a second reportL C Wilson, B A Kerr, R Wilkinson, et al.Infection and Immunity|June 11, 2014
Platelet endothelial cell adhesion molecule-1, a putative receptor for the adhesion of Streptococcus pneumoniae to the vascular endothelium of the blood-brain barrierFederico Iovino, Grietje Molema, Jetta J E BijlsmaEuropean Journal of Human Genetics : EJHG|May 30, 2003
Mutations in PAX1 may be associated with Klippel-Feil syndromeJ M McGaughran, A Oates, D Donnai, et al.European Journal of Human Genetics : EJHG|November 26, 1999
A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndromeM Tassabehji, M Carette, C Wilmot, 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.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.American Journal of Medical Genetics|February 15, 1992
Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)A M Norman, A P Read, J Clayton-Smith, et al.American Journal of Medical Genetics|May 15, 1994
Spondylocarpotarsal synostosis syndrome (with or without unilateral unsegmented bar)L O Langer, R J Gorlin, D Donnai, et al.Journal of Medical Genetics|March 1, 1993
Refining the genetic location of the gene for X linked hydrocephalus within Xq28M Jouet, E Feldman, J Yates, et al.Pageof 17