Showing results (51-60 of 129) with videos related to
Sort By:
Pageof 13
American Journal of Medical Genetics|May 1, 1987
Proteus syndrome: an expanded phenotypeR D Clark, D Donnai, J Rogers, et al.Prenatal Diagnosis|May 1, 1994
Examination of fetuses after induced abortion for fetal abnormality--a follow-up studyA Medeira, A Norman, J Haslam, et al.Journal of Medical Genetics|November 1, 1991
The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkageD Donnai, J Clayton-Smith, R J Gibbons, et al.Journal of Medical Genetics|November 1, 1990
Ankyloblepharon filiforme adnatum in trisomy 18 Edwards syndromeD G Evans, I D Evans, D Donnai, et al.Journal of Medical Genetics|October 1, 1981
Antenatal diagnosis of Niemann-Pick disease in a twin pregnancyP Donnai, D Donnai, R Harris, et al.Journal of Medical Genetics|November 5, 2002
De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and overlap with murine modelsE Elson, R Perveen, D Donnai, et al.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.European 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.Pageof 13