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Year | Number of Results |
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2001 | 1 |
2006 | 1 |
2011 | 1 |
2014 | 1 |
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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.
Am J Med Genet A. 2006 Nov 15;140(22):2401-15. doi: 10.1002/ajmg.a.31525.
Am J Med Genet A. 2006.
PMID: 17041943
Free PMC article.
Pattern of connexin 26 (GJB2) mutations causing sensorineural hearing impairment in Ghana.
Hamelmann C, Amedofu GK, Albrecht K, Muntau B, Gelhaus A, Brobby GW, Horstmann RD.
Hamelmann C, et al.
Hum Mutat. 2001;18(1):84-5. doi: 10.1002/humu.1156.
Hum Mutat. 2001.
PMID: 11439000
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Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population.
Kabahuma RI, Ouyang X, Du LL, Yan D, Hutchin T, Ramsay M, Penn C, Liu XZ.
Kabahuma RI, et al.
Int J Pediatr Otorhinolaryngol. 2011 May;75(5):611-7. doi: 10.1016/j.ijporl.2011.01.029. Epub 2011 Mar 9.
Int J Pediatr Otorhinolaryngol. 2011.
PMID: 21392827
Free PMC article.
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Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects.
Neocleous V, Costi C, Shammas C, Spanou E, Anastasiadou V, Tanteles GA, Phylactou LA.
Neocleous V, et al.
J Genet. 2014 Aug;93(2):471-6. doi: 10.1007/s12041-014-0365-0.
J Genet. 2014.
PMID: 25189242
Free article.
No abstract available.
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