These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
61 related articles for article (PubMed ID: 5021277)
1. 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]
2. 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]
3. A sociomedical study of deafmutes. Singh G; Singh SR; Indrayan A; Bagchi SC Indian J Med Res; 1973 Feb; 61(2):285-91. PubMed ID: 4759004 [No Abstract] [Full Text] [Related]
4. 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]
5. [Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children]. Bliumina MG; Moskovkina AG Vestn Otorinolaringol; 1980; (1):67-73. PubMed ID: 6990581 [No Abstract] [Full Text] [Related]
6. 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]
7. Evidence for autosomal recessive inheritance of the syndrome of renal tubular acidosis with deafness. Nance WE; Sweeney A Birth Defects Orig Artic Ser; 1971 Mar; 07(4):70-2. PubMed ID: 5173352 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. 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]
11. Vialetto-Van Laere syndrome in two sisters born to consanguineous parents. RamachandranNair R; Parameswaran M; Girija AS Pediatr Neurol; 2004 May; 30(5):354-5. PubMed ID: 15165639 [TBL] [Abstract][Full Text] [Related]
12. A genetic study of familial deafness. Dar H; Winter ST Isr J Med Sci; 1969; 5(6):1219-26. PubMed ID: 5365605 [No Abstract] [Full Text] [Related]
13. 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]
15. 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]
16. 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]
18. 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]
19. DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3. Ali RA; Rehman AU; Khan SN; Husnain T; Riazuddin S; Friedman TB; Ahmed ZM; Riazuddin S Clin Genet; 2012 May; 81(5):498-500. PubMed ID: 22211675 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]