Application of Allele-Specific Primer Extension-Based Microarray for Simultaneous Multi-Gene Mutation Screening in Patients With Non-Syndromic Hearing Loss

International Journal of Molecular Medicine - Greece
doi 10.3892/ijmm_00000347
Full Text
Abstract

Available in full text

Date
Authors

Unknown

Publisher

Spandidos Publications

Related search

Screening of GJB6 Gene for the 342-Kb Deletion in Patients From Jordan With Non Syndromic Hearing Loss

International Journal of Human Genetics
Genetics
2005English

Mutations of the Connexin 26 Gene in Families With Non-Syndromic Hearing Loss

Molecular Medicine Reports
OncologyGeneticsMolecular BiologyBiochemistryCancer ResearchMolecular Medicine
2011English

Q829X, a Novel Mutation in the Gene Encoding Otoferlin (OTOF), Is Frequently Found in Spanish Patients With Prelingual Non-Syndromic Hearing Loss

Journal of Medical Genetics
Genetics
2002English

Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss

International Journal of Human Genetics
Genetics
2006English

Prevalence of Connexin 26 Mutations in Patients From Jordan With Non Syndromic Hearing Loss

International Journal of Human Genetics
Genetics
2006English

Mutation of COL11A2 Causes Autosomal Recessive Non-Syndromic Hearing Loss at the DFNB53 Locus

Journal of Medical Genetics
Genetics
2005English

TBL1Y: A New Gene Involved in Syndromic Hearing Loss

European Journal of Human Genetics
Genetics
2018English

Comprehensive Analysis of Syndromic Hearing Loss Patients in Japan

Scientific Reports
Multidisciplinary
2019English

GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss

Revista Romana de Medicina de Laborator
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy