Showing results (1-10 of 92) with videos related to
Sort By:
Pageof 10
Nature Genetics|November 1, 1994
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) geneM Tassabehji, V E Newton, A P ReadAmerican Journal of Medical Genetics|January 2, 1995
Waardenburg syndrome type II: phenotypic findings and diagnostic criteriaX Z Liu, V E Newton, A P ReadNature Genetics|August 1, 1994
A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1A E Hughes, V E Newton, X Z Liu, et al.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 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.The Journal of Laryngology and Otology|March 1, 1991
Sensorineural hearing loss and the Marinesco-Sjögren syndromeV E NewtonAudiology : Official Organ of the International Society of Audiology|January 1, 1983
Sound localisation in children with a severe unilateral hearing lossV E NewtonScandinavian Audiology|January 1, 1989
Waardenburg's syndrome: a comparison of biometric indices used to diagnose lateral displacement of the inner canthiV E NewtonPageof 10