Waardenburg Syndrome Type 2
What's New
Last Posted: Mar 10, 2023
- Genetic analysis of a Chinese family with members affected with Usher syndrome type II and Waardenburg syndrome type IV.
Wang Xueling, et al. International journal of pediatric otorhinolaryngology 2017 0 114-118 - Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese families.
Wang Li, et al. Molecular medicine reports 2017 0 (1) 172-178 - A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients.
Jalilian Nazanin, et al. International journal of molecular and cellular medicine 2018 0 (1) 17-23 - The clinical and genetic research of Waardenburg syndrome type I and II in Chinese families.
Liu Qin, et al. International journal of pediatric otorhinolaryngology 2019 0 109806 - The heterozygous EDNRB mutation in a Chinese family with Waardenburg syndrome type I.
Cheng Huan-Huan, et al. International journal of ophthalmology 2019 0 (9) 1507-1509 - Targeted next-generation sequencing identified a novel variant of SOX10 in a Chinese family with Waardenburg syndrome type 2.
Liu Xiao-Wen, et al. The Journal of international medical research 2020 0 (11) 300060520967540 - A Novel PAX3 Mutation in a Chinese Family with Waardenburg Syndrome Type 1.
Li Shuling, et al. Genetic testing and molecular biomarkers 2020 0 (5) 249-255 - A Novel Frameshift Variant of the MITF Gene in a Chinese Family with Waardenburg Syndrome Type 2.
Li Ying, et al. Molecular syndromology 2021 0 (4) 244-249 - A novel PAX3 mutation in a Chinese Han family with Waardenburg syndrome type 1.
Guo Min, et al. International journal of pediatric otorhinolaryngology 2021 0 110758 - Identification of six novel variants in Waardenburg syndrome type II by next-generation sequencing.
Ren Shumin, et al. Molecular genetics & genomic medicine 2020 0 (3) e1128
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- Page last reviewed:Feb 1, 2024
- Page last updated:May 18, 2024
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