139 related articles for article (PubMed ID: 12885337)
1. High incidence of profound deafness in an isolated community.
Zlotogora J; Barges S
Genet Test; 2003; 7(2):143-5. PubMed ID: 12885337
[TBL] [Abstract][Full Text] [Related]
2. The genetics of deafness.
Nance WE
Ment Retard Dev Disabil Res Rev; 2003; 9(2):109-19. PubMed ID: 12784229
[TBL] [Abstract][Full Text] [Related]
3. Genetic epidemiological studies of congenital/prelingual deafness in Turkey: population structure and mating type are major determinants of mutation identification.
Tekin M; Arici ZS
Am J Med Genet A; 2007 Jul; 143A(14):1583-91. PubMed ID: 17444514
[TBL] [Abstract][Full Text] [Related]
4. Sensorineural hearing loss in Jewish children born in Jerusalem.
Levi H; Tell L; Cohen T
Int J Pediatr Otorhinolaryngol; 2004 Oct; 68(10):1245-50. PubMed ID: 15364494
[TBL] [Abstract][Full Text] [Related]
5. Consanguinity and deafness in Omani children.
Khabori MA; Patton MA
Int J Audiol; 2008 Jan; 47(1):30-3. PubMed ID: 18196484
[TBL] [Abstract][Full Text] [Related]
6. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.
Denoyelle F; Marlin S; Weil D; Moatti L; Chauvin P; Garabédian EN; Petit C
Lancet; 1999 Apr; 353(9161):1298-303. PubMed ID: 10218527
[TBL] [Abstract][Full Text] [Related]
7. The fate of 12 recessive mutations in a single village.
Zlotogora J; Hujerat Y; Barges S; Shalev SA; Chakravarti A
Ann Hum Genet; 2007 Mar; 71(Pt 2):202-8. PubMed ID: 17331080
[TBL] [Abstract][Full Text] [Related]
8. Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population.
Walsh T; Abu Rayan A; Abu Sa'ed J; Shahin H; Shepshelovich J; Lee MK; Hirschberg K; Tekin M; Salhab W; Avraham KB; King MC; Kanaan M
Hum Genomics; 2006 Jan; 2(4):203-11. PubMed ID: 16460646
[TBL] [Abstract][Full Text] [Related]
9. Estimated number of loci for autosomal recessive severe nerve deafness within the Israeli Jewish population, with implications for genetic counseling.
Brownstein Z; Friedlander Y; Peritz E; Cohen T
Am J Med Genet; 1991 Dec; 41(3):306-12. PubMed ID: 1789284
[TBL] [Abstract][Full Text] [Related]
10. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.
Denoyelle F; Weil D; Maw MA; Wilcox SA; Lench NJ; Allen-Powell DR; Osborn AH; Dahl HH; Middleton A; Houseman MJ; Dodé C; Marlin S; Boulila-ElGaïed A; Grati M; Ayadi H; BenArab S; Bitoun P; Lina-Granade G; Godet J; Mustapha M; Loiselet J; El-Zir E; Aubois A; Joannard A; Levilliers J; Garabédian EN; Mueller RF; Gardner RJ; Petit C
Hum Mol Genet; 1997 Nov; 6(12):2173-7. PubMed ID: 9336442
[TBL] [Abstract][Full Text] [Related]
11. Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
Carrasquillo MM; Zlotogora J; Barges S; Chakravarti A
Hum Mol Genet; 1997 Nov; 6(12):2163-72. PubMed ID: 9328482
[TBL] [Abstract][Full Text] [Related]
12. Consanguinity among the Arab and Jewish populations in Israel.
Jaber L; Halpern GJ
Pediatr Endocrinol Rev; 2006 Aug; 3 Suppl 3():437-46. PubMed ID: 17551463
[TBL] [Abstract][Full Text] [Related]
13. Consanguinity and endogamy in Northern Tunisia and its impact on non-syndromic deafness.
Ben Arab S; Masmoudi S; Beltaief N; Hachicha S; Ayadi H
Genet Epidemiol; 2004 Jul; 27(1):74-9. PubMed ID: 15185405
[TBL] [Abstract][Full Text] [Related]
14. Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation.
Mesolella M; Tranchino G; Nardone M; Motta S; Galli V
Int J Pediatr Otorhinolaryngol; 2004 Aug; 68(8):995-1005. PubMed ID: 15236885
[TBL] [Abstract][Full Text] [Related]
15. Consanguinity in a population sample of Israeli Muslim Arabs, Christian Arabs and Druze.
Vardi-Saliternik R; Friedlander Y; Cohen T
Ann Hum Biol; 2002; 29(4):422-31. PubMed ID: 12160475
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel.
Basel-Vanagaite L; Taub E; Halpern GJ; Drasinover V; Magal N; Davidov B; Zlotogora J; Shohat M
Eur J Hum Genet; 2007 Feb; 15(2):250-3. PubMed ID: 17149387
[TBL] [Abstract][Full Text] [Related]
18. Origin and expansion of four different beta globin mutations in a single Arab village.
Zlotogora J; Hujerat Y; Zalman L; Barges S; Filon D; Koren A; Shalev SA; Chakravarti A
Am J Hum Biol; 2005; 17(5):659-61. PubMed ID: 16136542
[TBL] [Abstract][Full Text] [Related]
19. Nonsyndromal profound genetic deafness in childhood.
Cremers CW; Marres HA; van Rijn PM
Ann N Y Acad Sci; 1991; 630():191-6. PubMed ID: 1952589
[TBL] [Abstract][Full Text] [Related]
20. Causes of deafness in British Bangladeshi children: a prevalence twice that of the UK population cannot be accounted for by consanguinity alone.
Bajaj Y; Sirimanna T; Albert DM; Qadir P; Jenkins L; Cortina-Borja M; Bitner-Glindzicz M
Clin Otolaryngol; 2009 Apr; 34(2):113-9. PubMed ID: 19413608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
