Identification of a hot spot for microdeletions in patients with X- linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4-Reference-Cited by-同舟云学术

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Identification of a hot spot for microdeletions in patients with X- linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4

Published:1996-09-01 Issue:9 Volume:5 Page:1229-1235
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

de Kok Y.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/5/9/1229/1658529/5-9-1229.pdf

Cited by 139 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. Functional categorization of gene regulatory variants that cause Mendelian conditions;Human Genetics;2024-03-04

2. Genome sequencing detects a balanced pericentric inversion with breakpoints that impact the DMD and upstream region of POU3F4 genes;American Journal of Medical Genetics Part A;2023-11-06

3. Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review;Biomedicines;2023-06-12

4. Higher-order Chromatin Organization in Diseases, from Chromosomal Position Effect to Phenotype Variegation;Handbook of Epigenetics;2023

5. Considering gene therapy to protect from X‐linked deafness DFNX2 and associated neurodevelopmental disorders;Ibrain;2022-09-27

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