62 related articles for article (PubMed ID: 5465901)
1. [Selection of genes responsible for deafness].
Kaneko S
Nihon Jibiinkoka Gakkai Kaiho; 1970 Jul; 73(7):848-58. PubMed ID: 5465901
[No Abstract] [Full Text] [Related]
2. Epidemiological and genetic studies of congenital profound deafness in the general population of Sichuan, China.
Liu X; Xu L; Zhang S; Xu Y
Am J Med Genet; 1994 Nov; 53(2):192-5. PubMed ID: 7856647
[TBL] [Abstract][Full Text] [Related]
3. [Mode of inheritance of congenital deaf-mutism].
Hu DN; Qiu WQ; Wu BT; Fang LZ; Zhou F; Gu YP; Zhang QH; Yan JH
Yi Chuan Xue Bao; 1988; 15(4):303-8. PubMed ID: 3273676
[No Abstract] [Full Text] [Related]
4. 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]
5. 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]
6. Inherited congenital profound deafness in a genetic isolate.
Arias S
Birth Defects Orig Artic Ser; 1974; 10(10):230-43. PubMed ID: 4462634
[No Abstract] [Full Text] [Related]
7. Deafness among children in northern Israel: incidence and etiology.
Winter ST; Dar H
Isr J Med Sci; 1967; 3(6):894-8. PubMed ID: 5587581
[No Abstract] [Full Text] [Related]
8. 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]
9. [Marriage of blood relatives and congenital deafness].
Panakhian VM
Vestn Otorinolaringol; 2005; (2):22-4. PubMed ID: 16025928
[TBL] [Abstract][Full Text] [Related]
10. Genetic and environmental factors in profound prelingual deafness.
Brown KS
Med Clin North Am; 1969 Jul; 53(4):741-72. PubMed ID: 4894100
[No Abstract] [Full Text] [Related]
11. Genetic selection for deafness: the views of hearing children of deaf adults.
Mand C; Duncan RE; Gillam L; Collins V; Delatycki MB
J Med Ethics; 2009 Dec; 35(12):722-8. PubMed ID: 19948926
[TBL] [Abstract][Full Text] [Related]
12. Two types of congenital recessive deafness.
Mengel MC; Konigsmark BW; McKusick VA
Eye Ear Nose Throat Mon; 1969 May; 48(5):301-5. PubMed ID: 5779514
[No Abstract] [Full Text] [Related]
13. The Perrault syndrome: autosomal recessive ovarian dysgenesis with facultative, non-sex-limited sensorineural deafness.
Pallister PD; Opitz JM
Am J Med Genet; 1979; 4(3):239-46. PubMed ID: 517579
[TBL] [Abstract][Full Text] [Related]
14. An epidemiological and genetic study of congenital profound deafness in Tunisia (governorate of Nabeul).
Ben Arab S; Bonaïti-Pellié C; Belkahia A
J Med Genet; 1990 Jan; 27(1):29-33. PubMed ID: 2308153
[TBL] [Abstract][Full Text] [Related]
15. [Familial forms of deafness].
Gapanovich VIa; Timoshenko PA; Gorbachuk VD; Kachan AA; Lipnitskaia LN
Vestn Otorinolaringol; 1972; 34(6):35-7. PubMed ID: 4665370
[No Abstract] [Full Text] [Related]
16. [Epidemiologic study of 338 cases of deafness].
Fernández de Castro J
Rev Invest Salud Publica; 1970; 30(4):242-84. PubMed ID: 5516704
[No Abstract] [Full Text] [Related]
17. Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness.
Lezirovitz K; Pardono E; de Mello Auricchio MT; de Carvalho E Silva FL; Lopes JJ; Abreu-Silva RS; Romanos J; Batissoco AC; Mingroni-Netto RC
Eur J Hum Genet; 2008 Jan; 16(1):89-96. PubMed ID: 17851452
[TBL] [Abstract][Full Text] [Related]
18. A preliminary study on consanguinity and deafmutes.
Majumdar NK
J Indian Med Assoc; 1972 Feb; 58(3):78-83. PubMed ID: 5021277
[No Abstract] [Full Text] [Related]
19. The hereditary syndrome of congenital deafness and retinitis pigmentosa. (Usher's syndrome).
Kloepfer HW; Laguaite JK
Laryngoscope; 1966 May; 76(5):850-62. PubMed ID: 5937908
[No Abstract] [Full Text] [Related]
20. Symposium on sensorineural hearing loss in children: early detection and intervention. Genetic factors in deafness of early life.
Nance WE; Sweeney A
Otolaryngol Clin North Am; 1975 Feb; 8(1):19-48. PubMed ID: 1090886
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]