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2006, ISBN 1597560219, xiv, 136
Book
07/2011
Waardenburg syndrome (WS) is a rare autosomally inherited and genetically heterogeneous disorder of neural crest cell development with distinct cutaneous... 
Waardenburg syndrome type 3 | Waardenburg syndrome | Klein-Waardenburg syndrome
Web Resource
PLoS genetics, ISSN 1553-7390, 2011, Volume 7, Issue 7, pp. e1002114 - e1002114
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2007, Volume 81, Issue 6, pp. 1169 - 1185
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2015, Volume 97, Issue 5, pp. 647 - 660
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 10/2018, Volume 113, pp. 229 - 233
Waardenburg Syndrome (WS) as a congenital auditory-pigmentary syndrome is a clinically and genetically heterogeneous disorder. Based upon clinical... 
PAX3 | Novel variant | Waardenburg syndrome | Klein-Waardenburg syndrome | DEAFNESS-HAND SYNDROME | ISOFORMS | MITF | FAMILY | PAIRED DOMAIN | SYNDROME TYPE-I | OTORHINOLARYNGOLOGY | PEDIATRICS | SYNDROME TYPE-1 | MUTATIONS | INHERITANCE | Genetic disorders | Genes | Genetic research | Genetic engineering | Nucleotide sequencing | Gene expression | DNA sequencing | Index Medicus
Journal Article
Journal Article
Indian Journal of Nephrology, ISSN 0971-4065, 05/2018, Volume 28, Issue 3, pp. 226 - 228
Waardenburg syndrome (WS) is a rare genetic disorder characterized by varying degrees of hearing loss, pigmentary anomalies, and defects of other neural crest... 
white forelock | Waardenburg syndrome | Minimal change disease | Case studies | Dosage and administration | Diagnosis | Drug therapy | Klein-Waardenburg syndrome | Prednisolone | Urine | Hair | Deafness | Nephrology | Congenital diseases | Hearing impairment | Patients | Defects | Consortia | Microscopy | Consent | Rodents | Mutation | Case Report
Journal Article
Molecular Medicine Reports, ISSN 1791-2997, 01/2018, Volume 17, Issue 1, pp. 172 - 178
Journal Article
Indian Journal of Dermatology, Venereology and Leprology, ISSN 0378-6323, 07/2006, Volume 72, Issue 4, pp. 326 - 326
Waardenburg syndrome is a rare inherited and genetically heterogenous disorder of neural crest cell development. Four distinct subtypes showing marked... 
Waardenburg syndrome | Dystopia canthorum | Waardenburg Syndrome - diagnosis | Deafness - genetics | Pedigree | Waardenburg Syndrome - genetics | Humans | Female | Child | Waardenburg Syndrome - classification | Deafness - diagnosis | Case studies | Klein-Waardenburg syndrome | Index Medicus
Journal Article