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Case Reports- Waardenburg syndrome type 2 in an African patient, 12/2005
A thirty six year-old African man, born in the Southern part of Libya, presented with congenital deafness and white forelock, variable-sized hypopigmented,... 
Waardenburg syndrome type 2, White forelock, Bilateral iris hypochromia
Journal
Journal of Clinical Dermatology, ISSN 1000-4963, 08/2014, Volume 43, Issue 8, pp. 479 - 480
Journal Article
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
02/2010
Background: Waardenburg syndrome (WS) is a rare, autosomal dominant disorder characterized by congenital hearing loss; dystopia canthorum; broad nasal root;... 
Congenital sensorineural hearing loss | Waardenburg syndrome | White forelock
Web Resource
JAMA Pediatrics, ISSN 2168-6203, 03/2018, Volume 172, Issue 3, pp. 294 - 295
Journal Article
Saudi Journal of Ophthalmology, ISSN 1319-4534, 09/2019
Journal Article
Chinese Journal of Medical Genetics, ISSN 1003-9406, 05/2019, Volume 36, Issue 5, pp. 477 - 479
Journal Article
2006, ISBN 1597560219, xiv, 136
Book
Development (Cambridge), ISSN 0950-1991, 02/2015, Volume 142, Issue 4, pp. 620 - 632
Melanocyte development provides an excellent model for studying more complex developmental processes. Melanocytes have an apparently simple aetiology,... 
MITF | Neural crest | Melanoma | Stem cells | ENDOTHELIN RECEPTOR-B | STEM-CELLS | HAIR FOLLICLE | WAARDENBURG-SYNDROME | MITF GERMLINE MUTATION | MELANOBLAST MIGRATION | DEVELOPMENTAL BIOLOGY | NEURAL CREST CELLS | MICROPHTHALMIA TRANSCRIPTION FACTOR | ULTRAVIOLET-RADIATION | MACROPHAGE-LIKE MELANOCYTES
Journal Article
Online Journal of Health & Allied Sciences, 07/2015, Volume 14, Issue 2
We report a case of blue eyes of Waardenburg Syndrome, with findings of hypopigmentation on the posterior pole 
Blue eyes | Waardenburg Syndrome
Journal Article
CANCER RESEARCH, ISSN 0008-5472, 05/2019, Volume 79, Issue 10, pp. 2649 - 2661
Histone modifications, largely regulated by histone acetyl-transferases (HAT) and histone deacetylases, have been recognized as major regulatory mechanisms... 
METASTATIC MELANOMA | ONCOLOGY | WAARDENBURG-SYNDROME | DNA-DAMAGE RESPONSE | DOWN-REGULATION | RESISTANCE | SENESCENCE | FOXM1 | TRANSCRIPTION FACTOR | CANCER | CELL
Journal Article
Acta Oto-Laryngologica, ISSN 0001-6489, 10/2019, Volume 139, Issue 10, pp. 870 - 875
Background: Deletions of the interstitial 2q36 are uncommon and associated with varying phenotypes. However, the list of currently known phenotypes is still... 
2q36.1-2q36.3 | brachydactyly | Syndromic hearing loss | microdeletion | 3 | OTORHINOLARYNGOLOGY | PAX3 | 2q36 | MUTATIONS | 1-2q36 | WAARDENBURG SYNDROME
Journal Article
International Journal of Ophthalmology, ISSN 2222-3959, 09/2019, Volume 12, Issue 9, pp. 1507 - 1509
The genovariation of endothelin receptor type B (EDNRB) was identified in a Chinese family with Waardenburg syndrome type I (WS1) in the present study. WS1 was... 
Waardenburg syndrome type I | Chinese family | EDNRB | gene mutation
Journal Article
Dermatology Online Journal, ISSN 1087-2108, 2018, Volume 24, Issue 2
Waardenburg Syndrome (WS) is a condition characterized by pigmentary changes of the hair or skin, hearing loss, heterochromia iridis, and dystopia canthorum.... 
Heterochromia iridis | Waardenburg syndrome | Dystopia canthorum | Hearing loss | Nevus depigmentosus
Journal Article
Gene, ISSN 0378-1119, 07/2019, Volume 704, pp. 86 - 90
The purpose of this study is to profile the clinical and genetic features of Japanese Waardenburg syndrome (WS) patients and validate the W index. Sixteen... 
Type | Waardenburg syndrome | Classification | Diagnosis | Mutation | Dystopia canthorum | W index | Hearing loss | GENETICS & HEREDITY | MUTATIONS | Genetic research | Genetic screening | Genetic disorders
Journal Article
International Journal of Circumpolar Health, ISSN 1239-9736, 01/2019, Volume 78, Issue 1, p. 1630219
Waardenburg syndrome (WS) is an orphan genetic disease with autosomal dominant pattern of inheritance characterised by varying degrees of hearing loss... 
MITF | Waardenburg syndrome | Sakha Republic | Eastern Siberia | Russia
Journal Article
Journal of pediatric health care : official publication of National Association of Pediatric Nurse Associates & Practitioners, ISSN 0891-5245, 07/2019
Waardenburg syndrome (WS) is a rare genetic disorder that is further divided into four subtypes with distinguishing clinical manifestations, categorized by... 
Journal Article
European Journal of Pediatric Dermatology, ISSN 1122-7672, 10/2016, Volume 26, Issue 4, pp. 216 - 219
Journal Article
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