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■ Search Result - Abbreviation : GJB2

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Abbreviation: GJB2
Appearance Frequency: 85 time(s)
Long forms: 8

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
gap junction protein beta 2
(41 times)
Otolaryngology
(8 times)
Cx26 (4 times)
HI (4 times)
HL (4 times)
1998 Connexin-26 mutations in sporadic and inherited sensorineural deafness.
gap junction beta-2
(29 times)
Otolaryngology
(9 times)
Cx26 (5 times)
NSHL (5 times)
SNHL (4 times)
2001 Nonradioactive detection of the common Connexin 26 167delT and 35delG mutations and frequencies among Ashkenazi Jews.
gap junction beta-2 protein
(5 times)
Medicine
(3 times)
GJB3 (2 times)
ARNSHL (1 time)
HL (1 time)
2015 Residual Hearing in DFNB1 Deafness and Its Clinical Implication in a Korean Population.
gap junction beta-2 gene
(4 times)
Genetics, Medical
(2 times)
ARNSHL (1 time)
Cx26 (1 time)
GJP (1 time)
2001 Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss.
gap junction protein, beta 2, 26 kDa
(3 times)
Molecular Biology
(2 times)
Cx26 (2 times)
CI (1 time)
GER (1 time)
2011 Detection of the GJB2 Mutation in Iranian Children with Hearing Loss Treated with Cochlear Implantation.
gap-junction B2
(1 time)
Otolaryngology
(1 time)
--- 2008 [Connexin gene 26 (GJB2) mutations in patients with hereditary non-syndromic sensorineural loss of hearing in the Republic of Sakha (Yakutia)].
Gjb2-CKO
(1 time)
Natural Science Disciplines
(1 time)
--- 2016 ACEMg Diet Supplement Modifies Progression of Hereditary Deafness.
GJB2-negative
(1 time)
Genetics, Medical
(1 time)
ARNSHL (1 time)
TMC1 (1 time)
2005 Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss.