These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Hereditary sensorineural hearing loss: advances in molecular genetics and mutation analysis. Schrijver I; Gardner P Expert Rev Mol Diagn; 2006 May; 6(3):375-86. PubMed ID: 16706740 [TBL] [Abstract][Full Text] [Related]
4. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature. Berrettini S; Forli F; Passetti S; Rocchi A; Pollina L; Cecchetti D; Mancuso M; Siciliano G Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147 [TBL] [Abstract][Full Text] [Related]
5. [Genetic and audiological characters of a Chinese family with non-syndromic hereditary hearing loss]. Jin Z; Cheng J; Lu Y; Li J; Sun Y; Yuan H; Han D Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Feb; 25(4):158-61. PubMed ID: 21563462 [TBL] [Abstract][Full Text] [Related]
6. [Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss]. Düzcan F; Wollnik B; Tepeli E; Ardiç FN; Uyguner O; Bağci H Kulak Burun Bogaz Ihtis Derg; 2003 Sep; 11(3):85-8. PubMed ID: 14699249 [TBL] [Abstract][Full Text] [Related]
7. Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population. Riga M; Psarommatis I; Lyra Ch; Douniadakis D; Tsakanikos M; Neou P; Apostolopoulos N Int J Pediatr Otorhinolaryngol; 2005 Apr; 69(4):449-55. PubMed ID: 15763280 [TBL] [Abstract][Full Text] [Related]
8. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene. Yan X; Wang X; Wang Z; Sun S; Chen G; He Y; Mo JQ; Li R; Jiang P; Lin Q; Sun M; Li W; Bai Y; Zhang J; Zhu Y; Lu J; Yan Q; Li H; Guan MX J Med Genet; 2011 Oct; 48(10):682-90. PubMed ID: 21931169 [TBL] [Abstract][Full Text] [Related]
9. [Rapid genetic diagnosis of patients with non-syndromic sensorineural hearing loss]. Zhang W; Gong S; Huang L; Liu B; Zhao L Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Jul; 25(13):593-6. PubMed ID: 21949990 [TBL] [Abstract][Full Text] [Related]
10. Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). McGuirt WT; Prasad SD; Griffith AJ; Kunst HP; Green GE; Shpargel KB; Runge C; Huybrechts C; Mueller RF; Lynch E; King MC; Brunner HG; Cremers CW; Takanosu M; Li SW; Arita M; Mayne R; Prockop DJ; Van Camp G; Smith RJ Nat Genet; 1999 Dec; 23(4):413-9. PubMed ID: 10581026 [TBL] [Abstract][Full Text] [Related]
11. [Forms of monosymptomatic hereditary sensorineural hearing loss and deafness in the Leipzig area]. Oeken J; König E HNO; 1993 Jun; 41(6):301-10. PubMed ID: 8365917 [TBL] [Abstract][Full Text] [Related]
12. Molecular analysis of hair cells in sensorineural hearing loss. Feng X; Qin Z Audiol Neurootol; 2014; 19(4):267-74. PubMed ID: 25228060 [TBL] [Abstract][Full Text] [Related]
13. Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes. Stinckens C; Ensink R; Feenstra L; Fryns JP; Cremers C Int J Pediatr Otorhinolaryngol; 1997 Jan; 38(3):237-45. PubMed ID: 9051428 [TBL] [Abstract][Full Text] [Related]
14. A comprehensive network and pathway analysis of human deafness genes. Stamatiou GA; Stankovic KM Otol Neurotol; 2013 Jul; 34(5):961-70. PubMed ID: 23770690 [TBL] [Abstract][Full Text] [Related]
16. Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness. Xia W; Liu F; Ma D Front Med; 2016 Jun; 10(2):137-42. PubMed ID: 27142990 [TBL] [Abstract][Full Text] [Related]
17. Vestibular and hearing loss in genetic and metabolic disorders. Gasparini P; Estivill X; Fortina P Curr Opin Neurol; 1999 Feb; 12(1):35-9. PubMed ID: 10097882 [TBL] [Abstract][Full Text] [Related]
18. The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations. Yan D; Kannan-Sundhari A; Vishwanath S; Qing J; Mittal R; Kameswaran M; Liu XZ Genet Test Mol Biomarkers; 2015 Sep; 19(9):512-27. PubMed ID: 26186295 [TBL] [Abstract][Full Text] [Related]
19. [Advances in studies on genetics of syndromes combining sensorineural hearing loss with scoliosis]. Wu K; Li Z; Zhang Q Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Jun; 35(6):556-562. PubMed ID: 34304520 [No Abstract] [Full Text] [Related]
20. Human nonsyndromic sensorineural deafness. Friedman TB; Griffith AJ Annu Rev Genomics Hum Genet; 2003; 4():341-402. PubMed ID: 14527306 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]