Results 91 to 100 of about 578 (106)

Review and update of mutations causing Waardenburg syndrome

Human Mutation, 2010
Veronique Pingault, Sandrine Marlin, Nadege Bondurand   +2 more
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Temporal bone abnormalities associated with hearing loss in waardenburg syndrome

Laryngoscope, 2010
Robert J Hopkin, Daniel Choo
exaly  

Phenotypic diversity and genetic complexity of PAX3‐related Waardenburg syndrome

American Journal of Medical Genetics, Part A, 2020
Priyanka Upadhyai, Dhanya L Narayanan, Nutan Kamath   +2 more
exaly  

Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome

Pediatric Dermatology, 2019
Mohammed D Saleem
exaly  

Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome

American Journal of Medical Genetics, Part A, 2003
Hulya Kayserili
exaly  

Hearing loss in Waardenburg syndrome: a systematic review

Clinical Genetics, 2016
Frederic Acke, Paul J Coucke, Ingeborg Jm Dhooge   +2 more
exaly  

Otopathology in a Case of Type I Waardenburg's Syndrome

Annals of Otology, Rhinology and Laryngology, 2001
Joseph B Nadol Jr
exaly  

Waardenburg syndrome: Clinical differentiation between types I and II

American Journal of Medical Genetics Part A, 2003
Eliete Pardono, Paulo A Otto
exaly  

Worldwide Distribution of Waardenburg Syndrome

Annals of Otology, Rhinology and Laryngology, 2003
exaly  

Waardenburg syndrome, Hirschsprung megacolon, and Marcus Gunn ptosis

American Journal of Medical Genetics Part A, 1987
exaly