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7. 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]
8. 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]
9. A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Friedman TB; Liang Y; Weber JL; Hinnant JT; Barber TD; Winata S; Arhya IN; Asher JH Nat Genet; 1995 Jan; 9(1):86-91. PubMed ID: 7704031 [TBL] [Abstract][Full Text] [Related]
10. [Autosomal recessive inheritance of hydrocephalus with stenosis of the duct of Sylvius]. Petrus M; Dutau G; Rochiccioli P J Genet Hum; 1981 Jun; 29(2):155-60. PubMed ID: 7328410 [No Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene. Jain PK; Lalwani AK; Li XC; Singleton TL; Smith TN; Chen A; Deshmukh D; Verma IC; Smith RJ; Wilcox ER Genomics; 1998 Jun; 50(2):290-2. PubMed ID: 9653658 [TBL] [Abstract][Full Text] [Related]
15. Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome. Liburd N; Ghosh M; Riazuddin S; Naz S; Khan S; Ahmed Z; Riazuddin S; Liang Y; Menon PS; Smith T; Smith AC; Chen KS; Lupski JR; Wilcox ER; Potocki L; Friedman TB Hum Genet; 2001 Nov; 109(5):535-41. PubMed ID: 11735029 [TBL] [Abstract][Full Text] [Related]
17. [Marriage of blood relatives and congenital deafness]. Panakhian VM Vestn Otorinolaringol; 2005; (2):22-4. PubMed ID: 16025928 [TBL] [Abstract][Full Text] [Related]
18. A form of sensorineural deafness is determined by a mitochondrial and an autosomal locus: evidence from pedigree segregation analysis. Bu X; Shohat M; Jaber L; Rotter JI Genet Epidemiol; 1993; 10(1):3-15. PubMed ID: 8472932 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Autosomal recessive "uncomplicated" profound childhood deafness in an Arabic family with high consanguinity. Kabarity A; Al-Awadi SA; Farag TI; Mallalah G Hum Genet; 1981; 57(4):444-6. PubMed ID: 7286990 [No Abstract] [Full Text] [Related] [Next] [New Search]