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by Tian, H and Wang, L and Gao, F and Liang, W and Peng, K.A
Clinical Otolaryngology, ISSN 1749-4478, 10/2018, Volume 43, Issue 5, pp. 1379 - 1383
Journal Article
Journal Article
Journal Article
Singapore medical journal, ISSN 0037-5675, 09/2006, Volume 47, Issue 9, pp. 822 - 4; quiz 825
Journal Article
Auris Nasus Larynx, ISSN 0385-8146, 2017, Volume 45, Issue 1, pp. 26 - 32
Abstract Objective Presenting the clinical features and treatment options for incomplete partition type-III. Methods Nine primary and 1 revision incomplete... 
Otolaryngology | Fixation | Cochlear hypoplasia | Inner ear malformations | Stapedotomy | Sensorineural hearing loss | Congenital stapes | X-LINKED DEAFNESS | STAPES GUSHER | INNER-EAR | OTORHINOLARYNGOLOGY | MIXED DEAFNESS | Index Medicus
Journal Article
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, ISSN 0165-5876, 01/2018, Volume 104, pp. 94 - 97
Here, we report a novel hemizygous transition c.975G > A (p.Trp325*) in POU3F4 gene (Xq21) found in two deaf half-brothers from one Yakut family (Eastern... 
DOMAIN | SENSORINEURAL HEARING-LOSS | Inner ear abnormality | X-linked recessive deafness | PERILYMPHATIC GUSHER | PHENOTYPE | IDENTIFICATION | LOCUS | POU3F4 | Russia | DELETION | REGION | OTORHINOLARYNGOLOGY | DFNX2 | Yakuts | PEDIATRICS | MUTATIONS | MIXED DEAFNESS | Eastern Siberia
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2014, Volume 9, Issue 10, pp. e109043 - e109043
Journal Article
Clinical Genetics, ISSN 0009-9163, 12/2009, Volume 76, Issue 6, pp. 558 - 563
X-linked deafness is a rare cause of hereditary isolated hearing impairment estimated as at least 1% or 2% of the non-syndromic hearing loss. To date, four... 
DFN3 | Female | Carrier | Hearing loss | POU3F4 | HEARING-LOSS | carrier | X-LINKED DEAFNESS | MOUSE MODEL | GENETICS & HEREDITY | GENE POU3F4 | female | GUSHER | MIXED DEAFNESS | Hearing Loss | Females | Genotype & phenotype | Mutation | Phenotype | POU Domain Factors - genetics | Humans | Middle Aged | Adult | Audiometry, Pure-Tone | Genotype | Heterozygote | Tomography, X-Ray Computed | Mutation - genetics
Journal Article
Human Mutation, ISSN 1059-7794, 02/2013, Volume 34, Issue 2, pp. 309 - 316
Journal Article