92 related articles for article (PubMed ID: 10981905)
21. Deafness and mutations in the connexin 26 gene.
Zlotogora J
N Engl J Med; 1999 Apr; 340(16):1288. PubMed ID: 10215495
[No Abstract] [Full Text] [Related]
22. Connexin 26 mutations: the first practical genetic marker of inherited hearing loss.
Perry CF
Med J Aust; 2001 Aug; 175(4):182-3. PubMed ID: 11587274
[No Abstract] [Full Text] [Related]
23. [Genetic deafness].
Vincent C
Rev Med Interne; 2011 Jun; 32 Suppl 1():S2-4. PubMed ID: 21549459
[No Abstract] [Full Text] [Related]
24. [Genetic diagnosis of deafness].
Usami S
Nihon Rinsho; 2005 Dec; 63 Suppl 12():258-63. PubMed ID: 16416804
[No Abstract] [Full Text] [Related]
25. Deaf intermarriage has limited effect on the prevalence of recessive deafness and no effect on underlying allelic frequency.
Braun DC; Jain S; Epstein E; Greenwald BH; Herold B; Gray M
PLoS One; 2020; 15(11):e0241609. PubMed ID: 33147256
[TBL] [Abstract][Full Text] [Related]
26. Molecular mechanism of a frequent genetic form of deafness.
Michel V; Hardelin JP; Petit C
N Engl J Med; 2003 Aug; 349(7):716-7. PubMed ID: 12917317
[No Abstract] [Full Text] [Related]
27. Selection for deafness?
Meyer CG; Amedofu GK; Brandner JM; Pohland D; Timmann C; Horstmann RD
Nat Med; 2002 Dec; 8(12):1332-3. PubMed ID: 12457154
[No Abstract] [Full Text] [Related]
28. Genetic screening for deafness.
Smith RJ; Hone S
Pediatr Clin North Am; 2003 Apr; 50(2):315-29. PubMed ID: 12809325
[TBL] [Abstract][Full Text] [Related]
29. Auditory function and the M34T allele of connexin 26.
Griffith AJ; Friedman TB
Arch Otolaryngol Head Neck Surg; 2002 Jan; 128(1):94. PubMed ID: 11784272
[No Abstract] [Full Text] [Related]
30. Impact of genetic counseling and Connexin-26 and Connexin-30 testing on deaf identity and comprehension of genetic test results in a sample of deaf adults: a prospective, longitudinal study.
Palmer CG; Boudreault P; Baldwin EE; Sinsheimer JS
PLoS One; 2014; 9(11):e111512. PubMed ID: 25375116
[TBL] [Abstract][Full Text] [Related]
31. Genetic evaluation and counseling for congenital deafness.
Green GE; Cunniff C
Adv Otorhinolaryngol; 2002; 61():230-40. PubMed ID: 12408089
[No Abstract] [Full Text] [Related]
32. DFNA3.
Denoyelle F; Weil D; Levilliers J; Petit C
Adv Otorhinolaryngol; 2000; 56():78-83. PubMed ID: 10868217
[No Abstract] [Full Text] [Related]
33. [New molecular genetic knowledge on development of hereditary deafness].
Pfister M
HNO; 1998 Sep; 46(9):782-4. PubMed ID: 9816530
[No Abstract] [Full Text] [Related]
34. Motors, channels and the sounds of silence.
Avraham KB
Nat Med; 1997 Jun; 3(6):608-9. PubMed ID: 9176483
[No Abstract] [Full Text] [Related]
35. Deafness-associated mutation opens the gate to understanding.
Sedwick C
J Gen Physiol; 2018 May; 150(5):647. PubMed ID: 29685927
[TBL] [Abstract][Full Text] [Related]
36. Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study.
Boudreault P; Baldwin EE; Fox M; Dutton L; Tullis L; Linden J; Kobayashi Y; Zhou J; Sinsheimer JS; Sininger Y; Grody WW; Palmer CG
J Deaf Stud Deaf Educ; 2010; 15(3):209-27. PubMed ID: 20488870
[TBL] [Abstract][Full Text] [Related]
37. PGD: new ethical challenges.
Robertson J
Nat Rev Genet; 2003 Jan; 4(1):6. PubMed ID: 12528685
[No Abstract] [Full Text] [Related]
38. Some deafness-causing mutations can be silenced with the appropriate gene partner.
Wilcox E; Riazuddin S; Riazuddin S
ScientificWorldJournal; 2001 May; 1():202-3. PubMed ID: 12805671
[TBL] [Abstract][Full Text] [Related]
39. Effect of pre-test genetic counseling for deaf adults on knowledge of genetic testing.
Baldwin EE; Boudreault P; Fox M; Sinsheimer JS; Palmer CG
J Genet Couns; 2012 Apr; 21(2):256-72. PubMed ID: 21818696
[TBL] [Abstract][Full Text] [Related]
40. The double life of connexin channels: single is a treat.
Bruzzone R
J Invest Dermatol; 2015 Apr; 135(4):940-943. PubMed ID: 25785946
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]