Cochlear implantation in 13q deletion syndrome
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology
Reference12 articles.
1. Chapter 68. Cochlear Implants;Gluth,2012
2. Chromosome deletion in a case of retinoblastoma;Lele;Ann Hum Genet,1963
3. Genotype–phenotype correlations in patients with retinoblastoma and interstitial 13q deletions;Mitter;Eur J Hum Genet,2011
4. 13q Deletion and central nervous system anomalies: further insights from karyotype–phenotype analyses of 14 patients;Ballarati;J Med Genet,2007
5. Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients;Alvarez;J Med Genet,2003
Cited by 2 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. Efnb2 haploinsufficiency induces early gap junction plaque disassembly and endocytosis in the cochlea;Brain Research Bulletin;2021-09
2. EFNB2haploinsufficiency causes a syndromic neurodevelopmental disorder;Clinical Genetics;2018-03-15
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