Relation between choice of partner and high frequency of connexin-26 deafness
- 1 August 2000
- journal article
- Published by Elsevier in The Lancet
- Vol. 356 (9228) , 500-501
- https://doi.org/10.1016/s0140-6736(00)02565-4
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Carrier Rates in the Midwestern United States for GJB2 Mutations Causing Inherited DeafnessJAMA, 1999
- Three novel connexin26 gene mutations in autosomal recessive nonsyndromic deafnessNeuroReport, 1999
- Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counsellingThe Lancet, 1999
- Connexin 26 gene mutation and autosomal recessive deafnessThe Lancet, 1998
- Connexin-26 mutations in sporadic and inherited sensorineural deafnessThe Lancet, 1998
- Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessNature, 1997
- XV.—The Correlation between Relatives on the Supposition of Mendelian Inheritance.Transactions of the Royal Society of Edinburgh, 1919