130 related articles for article (PubMed ID: 1789284)
1. 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]
2. Genetic heterogeneity study of non-syndromic autosomal recessive sensorineural deafness within the Tunisian population.
Chaabani H; Ben Arab S; Chebbi K
Ann Genet; 1995; 38(3):158-61. PubMed ID: 8540687
[TBL] [Abstract][Full Text] [Related]
3. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.
Auslender N; Sharon D; Abbasi AH; Garzozi HJ; Banin E; Ben-Yosef T
Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5431-8. PubMed ID: 18055789
[TBL] [Abstract][Full Text] [Related]
4. Recurrence risks for near relatives of children with sensori-neural deafness.
Koehn D; Morgan K; Fraser FC
Genet Couns; 1990; 1(2):127-32. PubMed ID: 2080997
[TBL] [Abstract][Full Text] [Related]
5. Cultural transmission of a sign language when deafness is caused by recessive alleles at two independent loci.
Aoki K; Feldman MW
Theor Popul Biol; 1994 Feb; 45(1):101-20. PubMed ID: 8023314
[TBL] [Abstract][Full Text] [Related]
6. Consanguinity analysis of congenital deafness in Northern Israel.
Costeff H; Dar H
Am J Hum Genet; 1980 Jan; 32(1):64-8. PubMed ID: 7361765
[TBL] [Abstract][Full Text] [Related]
7. Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness.
Scott HS; Kudoh J; Wattenhofer M; Shibuya K; Berry A; Chrast R; Guipponi M; Wang J; Kawasaki K; Asakawa S; Minoshima S; Younus F; Mehdi SQ; Radhakrishna U; Papasavvas MP; Gehrig C; Rossier C; Korostishevsky M; Gal A; Shimizu N; Bonne-Tamir B; Antonarakis SE
Nat Genet; 2001 Jan; 27(1):59-63. PubMed ID: 11137999
[TBL] [Abstract][Full Text] [Related]
8. Consanguinity among parents of hearing-impaired children in relation to ethnic groups in the Jewish population of Jerusalem.
Feinmesser M; Tell L; Levi H
Audiology; 1989; 28(5):268-71. PubMed ID: 2803114
[TBL] [Abstract][Full Text] [Related]
9. Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?
Fares F; Badarneh K; Abosaleh M; Harari-Shaham A; Diukman R; David M
Prenat Diagn; 2008 Mar; 28(3):236-41. PubMed ID: 18264947
[TBL] [Abstract][Full Text] [Related]
10. Bloom syndrome and Fanconi's anemia: rate and ethnic origin of mutation carriers in Israel.
Peleg L; Pesso R; Goldman B; Dotan K; Omer M; Friedman E; Berkenstadt M; Reznik-Wolf H; Barkai G
Isr Med Assoc J; 2002 Feb; 4(2):95-7. PubMed ID: 11876000
[TBL] [Abstract][Full Text] [Related]
11. The impact of congenital malformations and Mendelian diseases on infant mortality in Israel.
Zlotogora J; Leventhal A; Amitai Y
Isr Med Assoc J; 2003 Jun; 5(6):416-8. PubMed ID: 12841013
[TBL] [Abstract][Full Text] [Related]
12. A novel SLC26A4 (PDS) deafness mutation retained in the endoplasmic reticulum.
Brownstein ZN; Dror AA; Gilony D; Migirov L; Hirschberg K; Avraham KB
Arch Otolaryngol Head Neck Surg; 2008 Apr; 134(4):403-7. PubMed ID: 18427006
[TBL] [Abstract][Full Text] [Related]
13. Genetic variation of three tetrameric tandem repeats in four distinct Israeli ethnic groups.
Amar A; Brautbar C; Motro U; Fisher T; Bonne-Tamir B; Israel S
J Forensic Sci; 1999 Sep; 44(5):983-6. PubMed ID: 10486950
[TBL] [Abstract][Full Text] [Related]
14. Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
Masmoudi S; Charfedine I; Rebeh IB; Rebai A; Tlili A; Ghorbel AM; Belguith H; Petit C; Drira M; Ayadi H
Clin Genet; 2004 Oct; 66(4):358-64. PubMed ID: 15355440
[TBL] [Abstract][Full Text] [Related]
15. Familial hydrocephalus of prenatal onset.
Zlotogora J; Sagi M; Cohen T
Am J Med Genet; 1994 Jan; 49(2):202-4. PubMed ID: 8116668
[TBL] [Abstract][Full Text] [Related]
16. Waardenburg syndrome in the Turkish deaf population.
Silan F; Zafer C; Onder I
Genet Couns; 2006; 17(1):41-8. PubMed ID: 16719276
[TBL] [Abstract][Full Text] [Related]
17. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
Guilford P; Ben Arab S; Blanchard S; Levilliers J; Weissenbach J; Belkahia A; Petit C
Nat Genet; 1994 Jan; 6(1):24-8. PubMed ID: 8136828
[TBL] [Abstract][Full Text] [Related]
18. Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.
Marazita ML; Ploughman LM; Rawlings B; Remington E; Arnos KS; Nance WE
Am J Med Genet; 1993 Jun; 46(5):486-91. PubMed ID: 8322805
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Hereditary hearing loss: new diagnostic possibilities].
Hergersberg M; Weigell-Weber M
Schweiz Med Wochenschr; 2000 Apr; 130(13):485-9. PubMed ID: 10812644
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
