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4. Molecular analysis of the POU3F4 gene in patients with clinical and radiographic evidence of X-linked mixed deafness with perilymphatic gusher. Friedman RA; Bykhovskaya Y; Tu G; Talbot JM; Wilson DF; Parnes LS; Fischel-Ghodsian N Ann Otol Rhinol Laryngol; 1997 Apr; 106(4):320-5. PubMed ID: 9109724 [TBL] [Abstract][Full Text] [Related]
5. Computed tomographic diagnosis of X-linked congenital mixed deafness, fixation of the stapedial footplate, and perilymphatic gusher. Talbot JM; Wilson DF Am J Otol; 1994 Mar; 15(2):177-82. PubMed ID: 8172298 [TBL] [Abstract][Full Text] [Related]
6. Novel mutation in the homeobox domain of transcription factor POU3F4 associated with profound sensorineural hearing loss. Schild C; Prera E; Lüblinghoff N; Arndt S; Aschendorff A; Birkenhäger R Otol Neurotol; 2011 Jun; 32(4):690-4. PubMed ID: 21555964 [TBL] [Abstract][Full Text] [Related]
7. X-linked mixed deafness syndrome with congenital fixation of the stapedial footplate and perilymphatic gusher (DFN3). Cremers CW; Snik AF; Huygen PL; Joosten FB; Cremers FP Adv Otorhinolaryngol; 2002; 61():161-7. PubMed ID: 12408080 [No Abstract] [Full Text] [Related]
8. X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21. Piussan C; Hanauer A; Dahl N; Mathieu M; Kolski C; Biancalana V; Heyberger S; Strunski V Am J Hum Genet; 1995 Jan; 56(1):224-30. PubMed ID: 7825582 [TBL] [Abstract][Full Text] [Related]
9. The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK. Brunner HG; van Bennekom A; Lambermon EM; Oei TL; Cremers WR; Wieringa B; Ropers HH Hum Genet; 1988 Dec; 80(4):337-40. PubMed ID: 2904400 [TBL] [Abstract][Full Text] [Related]
10. Preoperative computed tomography scan may fail to predict perilymphatic gusher. Krouchi L; Callonnec F; Bouchetemblé P; Tollard E; Dehesdin D; Marie JP Ann Otol Rhinol Laryngol; 2013 Jun; 122(6):374-7. PubMed ID: 23837389 [TBL] [Abstract][Full Text] [Related]
11. How to prevent a stapes gusher. Cremers CWRJ Adv Otorhinolaryngol; 2007; 65():278-284. PubMed ID: 17245059 [TBL] [Abstract][Full Text] [Related]
16. Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness. Reardon W; Roberts S; Phelps PD; Thomas NS; Beck L; Issac R; Hughes HE Am J Med Genet; 1992 Nov; 44(4):513-7. PubMed ID: 1442898 [TBL] [Abstract][Full Text] [Related]
17. Phenotype and genotype in females with POU3F4 mutations. Marlin S; Moizard MP; David A; Chaissang N; Raynaud M; Jonard L; Feldmann D; Loundon N; Denoyelle F; Toutain A Clin Genet; 2009 Dec; 76(6):558-63. PubMed ID: 19930154 [TBL] [Abstract][Full Text] [Related]
19. Clinical features of female heterozygotes in the X-linked mixed deafness syndrome (with perilymphatic gusher during stapes surgery). Cremers CW; Huygen PL Int J Pediatr Otorhinolaryngol; 1983 Nov; 6(2):179-85. PubMed ID: 6662621 [TBL] [Abstract][Full Text] [Related]
20. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. de Kok YJ; van der Maarel SM; Bitner-Glindzicz M; Huber I; Monaco AP; Malcolm S; Pembrey ME; Ropers HH; Cremers FP Science; 1995 Feb; 267(5198):685-8. PubMed ID: 7839145 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]