Showing results (1-10 of 1,834) with videos related to
Sort By:
Pageof 184
Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Family studies in Prader-Willi syndromeT Webb, C A Hardy, M Dahlitz, et al.Journal of Medical Genetics|March 1, 1995
A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndromeT Webb, D Clarke, C A Hardy, et al.Clinical Genetics|April 29, 1998
A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomesT Webb, C A Hardy, M King, et al.Clinical Genetics|April 1, 1996
A comparative study of X-inactivation in Rett syndrome probands and control subjectsT Webb, E WatkissJournal of Medical Genetics|August 1, 1993
Is skewed X inactivation responsible for symptoms in female carriers for adrenoleucodystrophy?E Watkiss, T Webb, S BundeyClinical Genetics|November 1, 1993
Neither uniparental disomy nor skewed X-inactivation explains Rett syndromeT Webb, E Watkiss, C G WoodsJournal of Medical Genetics|June 1, 1994
A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndromeS Vickers, M Dahlitz, C Hardy, et al.Journal of Medical Genetics|October 1, 1994
X inactivation patterns in female monozygotic twins and their familiesE Watkiss, T Webb, G Rysiecki, et al.Journal of Intellectual Disability Research : JIDR|January 16, 2004
Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndromeJ Whittington, A Holland, T Webb, et al.Pageof 184