Associated Papers
Deciphering potential causative factors for undiagnosed Waardenburg syndrome through multi-data integration.
Sun F et al.
Orphanet Journal of Rare Diseases, 2024
38844942 (PubMed )
Supplement: 13023_2024_3220_MOESM8_ESM.xls › Sheet1
Tenuous transcriptional threshold of human sex determination. II. SRY exploits water-mediated clamp at the edge of ambiguity.
Racca JD et al.
Frontiers in Endocrinology, 2022
36568077 (PubMed )
Supplement: DataSheet_1.pdf
[Analysis of genetic variation in patients with Waardenburg syndrome type Ⅱ by next generation sequencing].
Ren SM et al.
Zhonghua Yi Xue Za Zhi, 2020
Identification of six novel variants in Waardenburg syndrome type II by next-generation sequencing.
Ren S et al.
Molecular Genetics & Genomic Medicine, 2020
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