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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.
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.
Neuromolecular Medicine|January 5, 2006
Expression profiling of p53-target genes in copper-mediated neuronal apoptosisJacob W Vanlandingham, Nadine M Tassabehji, Rikki C Somers, et al.
American Journal of Human Genetics|July 1, 1993
Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndromeM Tassabehji, T Strachan, M Sharland, et al.
Brain Research|September 10, 2008
Zinc deficiency impairs neuronal precursor cell proliferation and induces apoptosis via p53-mediated mechanismsRikki S Corniola, Nadine M Tassabehji, Joan Hare, et al.
Nucleic Acids Research|December 11, 1994
Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene clusterM Tassabehji, T Strachan, M Anderson, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|September 25, 2001
Tremor in otosurgery: influence of physical strain on hand steadinessD Mürbe, K B Hüttenbrink, T Zahnert, et al.
FEBS Letters|March 10, 2007
GTF2IRD1 regulates transcription by binding an evolutionarily conserved DNA motif 'GUCE'P D Thompson, M Webb, W Beckett, et al.
Genomics|June 15, 1999
A complete physical contig and partial transcript map of the Williams syndrome critical regionE L Hockenhull, M J Carette, K Metcalfe, et al.
Human Molecular Genetics|July 1, 1997
Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosisM Tassabehji, K Metcalfe, D Donnai, et al.
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