A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 44 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Genomic Landscape of Branchio-Oto-Renal Syndrome through Whole-Genome Sequencing: A Single Rare Disease Center Experience in South Korea;International Journal of Molecular Sciences;2024-07-26
2. Phenotypic and molecular basis of SIX1 variants linked to non-syndromic deafness and atypical branchio-otic syndrome in South Korea;Scientific Reports;2023-07-21
3. A novel heterozygous SIX1 missense mutation resulted in non-syndromic unilateral hearing loss;Frontiers in Genetics;2022-11-22
4. A Case of Bilateral 3rd Branchial Cleft Anomaly Found in Patient with Branchio-Otic Syndrome;Journal of Clinical Otolaryngology Head and Neck Surgery;2022-09
5. Re-Examining the Cochlea in Branchio-Oto-Renal Syndrome: Genotype-Phenotype Correlation;American Journal of Neuroradiology;2022-01-20
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