相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Statistical study of 35delG mutation of GJB2 gene: A meta-analysis of carrier frequency
Nejat Mahdieh et al.
INTERNATIONAL JOURNAL OF AUDIOLOGY (2009)
Strong Linkage Disequilibrium for the Frequent GJB2 35delG Mutation in the Greek Population
Haris Kokotas et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population
Sung-Hee Han et al.
JOURNAL OF HUMAN GENETICS (2008)
Epidemiological study of nonsyndromic hearing loss in Sicilian newborns
M. Niceta et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2007)
High prevalences of carriers of the 35delG mutation of connexin 26 in the Mediterranean area
Gerard Lucotte
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY (2007)
Investigating the effects of prehistoric migrations in Siberia: genetic variation and the origins of Yakuts
Brigitte Pakendorf et al.
HUMAN GENETICS (2006)
Non-syndromic, autosomal-recessive deafness
MB Petersen et al.
CLINICAL GENETICS (2006)
GJB2 (Connexin 26) mutations are not a major cause of hearing loss in the Indonesian population
RL Snoeckx et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Further evidence for heterozygote advantage of GJB2 deafness mutations:: a link with cell survival
JEA Common et al.
JOURNAL OF MEDICAL GENETICS (2004)
High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals
D Wattanasirichaigoon et al.
CLINICAL GENETICS (2004)
Mitochondrial DNA and Y-chromosome variation in the Caucasus
I Nasidze et al.
ANNALS OF HUMAN GENETICS (2004)
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India -: art. no. e68
M RamShankar et al.
JOURNAL OF MEDICAL GENETICS (2003)
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians
D Yan et al.
HUMAN GENETICS (2003)
The prevalence of connexin 26 (GJB2) mutations in the Chinese population
XZ Liu et al.
HUMAN GENETICS (2002)
GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: A HuGE review
A Kenneson et al.
GENETICS IN MEDICINE (2002)
Frequency of the 35delG mutation of the connexin 26 gene (GJB2) in patients with non-syndromic recessive deafness from Bashkortostan and in ethnic groups of the Volga-Ural region
IM Khidiyatova et al.
MOLECULAR BIOLOGY (2002)
A common founder for the 35deIG GJB2 gene mutation in connexin 26 hearing impairment
L Van Laer et al.
JOURNAL OF MEDICAL GENETICS (2001)
Meta-analysis of GJB2 mutation 35delG frequencies in Europe
G Lucotte et al.
GENETIC TESTING (2001)
Connexin 26 (GJB2) mutations in the Turkish population:: implications for the origin and high frequency of the 35delG mutation in Caucasians
M Tekin et al.
HUMAN GENETICS (2001)
PCR test for diagnosis of the common CJB2 (connexin 26) 35delG mutation on dried blood spots and determination of the carrier frequency in France
G Lucotte et al.
MOLECULAR AND CELLULAR PROBES (2001)
On the origin and frequency of the 35delG allele in GJB2-linked deafness in Europe
A Anichkina et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2001)
Relation between choice of partner and high frequency of cannexin-26 deafness
WE Nance et al.
LANCET (2000)
Connexin26 mutations associated with nonsyndromic hearing loss
HJ Park et al.
LARYNGOSCOPE (2000)
High carrier frequency of the 35delG deafness mutation in European populations
P Gasparini et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2000)
Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene
R Rabionet et al.
HUMAN GENETICS (2000)
分享论文
