A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p

American Journal of Human Genetics

Volumn 61, Issue 4, 1997, Pages 924-927

  Brown, M R ^a   Tomek, M S ^a   Van Laer, L ^b   Smith, S ^c   Kenyon, J B ^c   Van Camp, G ^b   Smith, R J H ^a  

^a UNIVERSITY OF IOWA HEALTH CARE   (United States)

^b Department of Medical Genetics ^*  (Belgium)

^c BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; AUTORADIOGRAPHY; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 6P; GENE; GENE MAPPING; GENOTYPE; HEARING LOSS; HUMAN; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TANDEM REPEAT;

EID: 0030766420     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/514892     Document Type: Article

References (19)

1. Brunner HG, van Beersum SEC, Warman ML, Olsen BR, Ropers HH, Mariman CM (1994) A stickler syndrome gene is linked to chromosome 6 near the COL11A2 gene. Hum Mol Genet 3:1561-1564
2. Cao M, Thonnard J, Philippe M, Deggouj N, Osselaer JC, Gersdorff M, Tomasi JP (1996) HLA class II-associated genetic susceptibility in idiopathic progressive sensorineural hearing loss. Ann Otol Rhinol Laryngol 105:628-633
3. Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC (1994) Quantitative trait locus for reading disability on chromosome 6. Science 266:276-279
4. Chaib H, Lina-Granade G, Guilford P, Plauchu H, Levilliers J, Morgon A, Petit C (1994) A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval. Hum Mol Genet 3:2219-2222
5. Cottingham RW Jr, Idury RM, Schäffer AA (1993) Faster sequential genetic linkage computations. Am J Hum Genet 53:252-263
6. de Kok YJ, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, Pembrey ME, et al (1995) Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science 267:685-688
7. de Kok YJ, Vossenaar ER, Cremers WRJ, Dahl N, Laporte J, Hu LJ, Lacombe D, et al (1996) Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900kb proximal to the DFN3 gene POU3F4. Hum Mol Genet 5:1229-1235
8. Geschwind N, Galaburda A (1985) Cerebral lateralization: biological mechanisms, associations, and pathology. 1. A hypothesis and a program of research. Arch Neurol 42:428-459
9. Greinwald JH, Scott DA, Marietta JR, Carmi R, Manaligod J, Ramesh A, Zbar RI, et al. Construction of a PAC and YAC contig encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21. Genome Res (in press)
10. Grigorenko FL, Wood FB, Meyer MS, Hart LA, Speed WC, Shuster A, Pauls DL (1997) Susceptibility loci for distinct components of developmental dyslexia on chromosome 6 and 15. Am J Hum Genet 60:27-39
11. Grimberg J, Nawoschik S, Belluscio L, McKee R, Turck A, Eisenberg A (1989) A simple and efficient non-organic procedure for the isolation of genomic DNA from blood. Nucleic Acids Res 17:390
12. Guillaudeux T, Mattei MG, Depetris D, Le Bouteiller P, Pontarotti P (1993) In situ hybridization localizes the human OTF3 to chromosome 6p21.3-p22 and OTF3L to 12p13. Cytogenet Cell Genet 63:212-214
13. Hanson I, Gorman P, Lui VCH, Cheah KSE, Solomon E, Trowsdale J (1989) The human α2(XI) collagen gene (COL11A2) maps to the centromeric border of the major histocompatibility complex on chromosome 6. Genomics 5: 925-931
14. Kirschhofer K, Kenyon JB, Hoover DM, Franz P, Weipolthammer K, Wachtler F, Kimberling WJ (1996) Autosomal dominant congenital severe sensorineural hearing loss: localisation of a disease gene to chromosome 11q by linkage analysis in an Austrian family. Paper presented at the Second Workshop of the European Workgroup on Genetics of Hearing Impairment. Milan, October 11-13
15. Lyon MF, Searle AG (1990) Genetic variants and strains of the laboratory mouse. Oxford University Press, New York
16. Morton NE (1991) Genetic epidemiology of hearing impairment. Ann NY Acad Sci 630:16-21
17. Sheffield VC, Weber JL, Beutow KH, Murray JC, Even DA, Wiles K, Duyk GM, et al (1995) A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps. Hum Mol Genet 4:1837-1844
18. Van Camp G, Willems PJ, Smith RJH (1997) Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 60:758-764
19. Verhoeven K, van Camp G, Govaerts PJ, Balemans W, Schatteman I, Van Laer L, Smith RJH, et al (1997) A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24. Am J Hum Genet 60: 1168-1173