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Screening for gap junction protein beta-2 gene mutations in Malays with autosomal recessive, non-syndromic hearing loss, using denaturing high performance liquid chromatography.

Autor

Bin Alwi Zilfalil

veröffentlicht in: The Journal of Laryngology & Otology

Erscheinungsdatum: 2008-03-20

Hauptthema: Schwerhörigkeit, Hochleistungsflüssigkeitschromatographie

Zitiert Artikel 27

Datum

Titel

Autor

2007-06-01

GJB2 and GJB6 mutations in children with congenital cytomegalovirus infection.
2006-11-01

DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls
2005-05-01

GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations.

Hannie Kremer
2005-01-01

Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment

Suzanne M. Leal
2005-09-01

High prevalence of the W24X mutation in the gene encoding connexin-26 (GJB2) in Spanish Romani (gypsies) with autosomal recessive non-syndromic hearing loss

Ignacio del Castillo, Manuela Villamar, Luis Augusto Aguirre Pérez, Anna González-Neira
2005-09-01

Hearing screening of infants in Neonatal Unit, Hospital Universiti Sains Malaysia using transient evoked otoacoustic emissions.
2003-10-01

GJB2 mutations in the Swiss hearing impaired.
2003-06-01

Non-invasive screening for GJB2 mutations in buccal smears for the diagnosis of inherited hearing impairment
2003-07-01

Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario

Madhulika Kabra
2002-09-01

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

Drakoulis Yannoukakos, Irene Konstantopoulou
2002-08-16

The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.
2002-05-01

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.
2001-08-01

A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment

Caroline Van de Heyning, Paul Van de Heyning, Guy Van Camp
2001-11-01

GJB2 (connexin 26) mutations and childhood deafness in Thailand
2000-01-01

Prevalent connexin 26 gene (GJB2) mutations in Japanese
1999-02-01

A stepwise approach to the diagnosis and treatment of hereditary hearing loss
1999-10-01

Neonatal screening for hearing disorders in infants at risk: incidence, risk factors, and follow-up
1999-11-01

Confirmation of deafness in infancy
1998-11-01

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

Guy Van Camp, Thomas B. Friedman, Bronya J. B. Keats
1998-11-01

Hearing screening in at-risk neonate cohort.
1998-09-01

The Rhode Island Hearing Assessment Program: experience with statewide hearing screening (1993-1996)
1998-02-01

Universal infant hearing screening by automated auditory brainstem response measurement.
1998-12-01

The newborn with hearing loss: detection in the nursery
1997-09-01

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

Xavier Estivill i Pallejà
1996-07-01

Auditory brainstem response screening for hearing loss in high risk neonates
1996-01-01

Neonatal otoacoustic emission screening and the identification of deafness
1991-10-01

Neonatal at risk screening and the identification of deafness

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