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Nature|February 13, 1992
Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box geneM Tassabehji, A P Read, V E Newton, et al.Nature Genetics|January 1, 1993
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2M Tassabehji, A P Read, V E Newton, et al.Human Mutation|January 1, 1996
Fluorescent multiplex microsatellites used to define haplotypes associated with 75 CFTR mutations from the UK on 437 CF chromosomesD Hughes, A Wallace, J Taylor, et al.Human Immunology|October 1, 1991
Characterization of an expressible nonclassical class I HLA geneM A Pook, V Woodcock, M Tassabehji, et al.Human Molecular Genetics|July 1, 1994
PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouseM Tassabehji, V E Newton, K Leverton, et al.Human Molecular Genetics|June 13, 1998
An elastin gene mutation producing abnormal tropoelastin and abnormal elastic fibres in a patient with autosomal dominant cutis laxaM Tassabehji, K Metcalfe, J Hurst, et al.American Journal of Medical Genetics|June 24, 1998
Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental originY Q Wu, V R Sutton, E Nickerson, et al.Human Molecular Genetics|November 1, 1995
The mutational spectrum in Waardenburg syndromeM Tassabehji, V E Newton, X Z Liu, et al.Bioinformatics (Oxford, England)|July 21, 2004
Exploring Williams-Beuren syndrome using myGridR D Stevens, H J Tipney, C J Wroe, et al.American Journal of Human Genetics|January 23, 1999
Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypesM Tassabehji, K Metcalfe, A Karmiloff-Smith, et al.Pageof 4