Three Cases of Waardenburg Syndrome Type 2 in a Korean Family.
Joong Hyuk Choi, Sung Kyun Moon, Ki Hwang Lee, Ho Min Lew, Yoon Hee Chang
Korean J Ophthalmol. 2004;18(2):185-189. Published online 2004 Dec 30 DOI: https://doi.org/10.3341/kjo.2004.18.2.185
|
Citations to this article as recorded by
Concurrent Cardiac and Renal Anomalies in Waardenburg Syndrome Type 1: A Report of a Rare Case
Ameer Awashra, Ahmad Nouri, Thabet Zidan, Abdelrahman Sawalma, Fathi S Milhem, Dalia Marbo’
Cureus.2024;[Epub] CrossRef Can Waardenburg syndrome type 2 be explained by epigenetic mosaicism?
Rudolf Happle
American Journal of Medical Genetics Part A.2021; 185(4): 1304. CrossRef Case of Waardenburg Shah syndrome in a family with review of literature
Setty.L.N. Chandra Mohan
Journal of Otology.2018; 13(3): 105. CrossRef Identification of a Novel De Novo Variant in the PAX3 Gene in Waardenburg Syndrome by Diagnostic Exome Sequencing: The First Molecular Diagnosis in Korea
Mi-Ae Jang, Taeheon Lee, Junnam Lee, Eun-Hae Cho, Chang-Seok Ki
Annals of Laboratory Medicine.2015; 35(3): 362. CrossRef A Case of Waardenburg Syndrome Type 2 With Anisocoria
Seung Chan Lee
Journal of the Korean Ophthalmological Society.2010; 51(10): 1423. CrossRef Hereditary hypo/de‐pigmented dermatoses: An overview
Virendra N. Sehgal, Govind Srivastava
International Journal of Dermatology.2008; 47(10): 1041. CrossRef Hereditary hypo/de-pigmented dermatoses: An overview
Virendra N. Sehgal, Govind Srivastava
International Journal of Dermatology.2008; 0: 080521053359321. CrossRef
Retrotransposon insertion in
SILV
is responsible for merle patterning of the domestic dog
Leigh Anne Clark, Jacquelyn M. Wahl, Christine A. Rees, Keith E. Murphy
Proceedings of the National Academy of Sciences.2006; 103(5): 1376. CrossRef
|