Evaluation of dHPLC for CX26 Mutation Screening in Patients from Southern France with Sensorineural Deafness
Author:
Affiliation:
1. Laboratoire de Génétique Moléculaire, CHU Montpellier, France
2. Département de Génétique médicale, CHU Montpellier, France
3. Département ORL, CHU Montpellier, France
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/109065701753617507
Reference23 articles.
1. Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness
2. A highly sensitive, fast, and economical technique for mutation analysis in hereditary breast and ovarian cancers
3. Mutation analysis of the hamartin gene using denaturing high performance liquid chromatography
4. Diagnostic Testing for Rett Syndrome by DHPLC and Direct Sequencing Analysis of the MECP2 Gene: Identification of Several Novel Mutations and Polymorphisms
5. Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss
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1. Molecular screening of deafness in Algeria: High genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F;European Journal of Medical Genetics;2009-07
2. Molecular Diagnosis of Hearing Loss;Current Protocols in Human Genetics;2004-10
3. Mutation Detection of GJB2 Using IsoCode and Real-Time Quantitative Polymerase Chain Reaction With SYBR Green I Dye for Newborn Hearing Screening;The Laryngoscope;2004-07
4. Molecular epidemiology of DFNB1 deafness in France;BMC Medical Genetics;2004-03-06
5. Nonsyndromic 35 delG Mutation of the Connexin 26 Gene Associated With Deafness in Syndromic Children: Two Case Reports;The Laryngoscope;2004-03
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