64 related articles for article (PubMed ID: 16416804)
1. [Genetic diagnosis of deafness].
Usami S
Nihon Rinsho; 2005 Dec; 63 Suppl 12():258-63. PubMed ID: 16416804
[No Abstract] [Full Text] [Related]
2. Rapid umbilical cord diagnostic of hereditary profound hearing loss: how we do it.
Birkenhäger R; Maier W; Kunze M; Aschendorff A; Arndt S
Clin Otolaryngol; 2009 Aug; 34(4):374-6. PubMed ID: 19673989
[No Abstract] [Full Text] [Related]
3. Molecular diagnosis of genetic deafness.
Jonard L; Marlin S; Louha M; Bonnet C; Couderc R; Garabedian N; Denoyelle F;
Clin Biochem; 2011 May; 44(7):510-511. PubMed ID: 22036352
[No Abstract] [Full Text] [Related]
4. Clinical application of genetic testing for deafness.
Smith RJ
Am J Med Genet A; 2004 Sep; 130A(1):8-12. PubMed ID: 15368487
[TBL] [Abstract][Full Text] [Related]
5. [Molecular diagnosis of deafness].
Usami S
Nihon Rinsho; 2011 Feb; 69(2):357-67. PubMed ID: 21387690
[TBL] [Abstract][Full Text] [Related]
6. Mutation screening for deafness: more than simply another diagnostic test.
Smith RJ
Arch Otolaryngol Head Neck Surg; 2001 Aug; 127(8):941-2. PubMed ID: 11493202
[No Abstract] [Full Text] [Related]
7. Deafness genes in Israel: implications for diagnostics in the clinic.
Brownstein Z; Avraham KB
Pediatr Res; 2009 Aug; 66(2):128-34. PubMed ID: 19390476
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Genetic testing to identify deaf newborns.
Green GE; Smith RJ; Bent JP; Cohn ES
JAMA; 2000 Sep; 284(10):1245. PubMed ID: 10979110
[No Abstract] [Full Text] [Related]
10. 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]
11. A new era in the genetics of deafness.
Steel KP
N Engl J Med; 1998 Nov; 339(21):1545-7. PubMed ID: 9819455
[No Abstract] [Full Text] [Related]
12. EMQN Best Practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus.
Hoefsloot LH; Roux AF; Bitner-Glindzicz M;
Eur J Hum Genet; 2013 Nov; 21(11):1325-9. PubMed ID: 23695287
[No Abstract] [Full Text] [Related]
13. Connexin 26 gene mutation and autosomal recessive deafness.
Reardon W
Lancet; 1998 Feb; 351(9100):383-4. PubMed ID: 9482285
[No Abstract] [Full Text] [Related]
14. [From gene to disease: deafness and connexin 26].
Hoefsloot LH; Kemperman M; Cremers CW
Ned Tijdschr Geneeskd; 2002 Feb; 146(6):259-61. PubMed ID: 11865655
[TBL] [Abstract][Full Text] [Related]
15. Connexin 26 gene linked to a dominant deafness.
Denoyelle F; Lina-Granade G; Plauchu H; Bruzzone R; Chaïb H; Lévi-Acobas F; Weil D; Petit C
Nature; 1998 May; 393(6683):319-20. PubMed ID: 9620796
[No Abstract] [Full Text] [Related]
16. [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]
17. Relation between choice of partner and high frequency of connexin-26 deafness.
Nance WE; Liu XZ; Pandya A
Lancet; 2000 Aug; 356(9228):500-1. PubMed ID: 10981905
[TBL] [Abstract][Full Text] [Related]
18. Connexin mutations in deafness.
White TW; Deans MR; Kelsell DP; Paul DL
Nature; 1998 Aug; 394(6694):630-1. PubMed ID: 9716127
[No Abstract] [Full Text] [Related]
19. Deafness. Sounds from the cochlea.
Avraham KB
Nature; 1997 Dec; 390(6660):559-60. PubMed ID: 9403680
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]