Deafness locus DFNB16 is located on chromosome 15q13-q21 within a 5-cM interval flanked by markers D15S994 and D15S132 [9]

American Journal of Human Genetics

Volumn 64, Issue 4, 1999, Pages 1238-1241

  Villamar, M ^a   Del Castillo, I ^a   Valle, N ^a   Romero, L ^a   Moreno, F ^a  

^a HOSPITAL RAMÓN Y CAJAL   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CLINICAL ARTICLE; GENE LOCUS; GENETIC LINKAGE; HAPLOTYPE; HEARING IMPAIRMENT; HUMAN; INCIDENCE; LETTER; PERCEPTION DEAFNESS; PRIORITY JOURNAL;

EID: 0033364725     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302321     Document Type: Letter

References (11)

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2. L Bergstrom WG Hemenway MP Downs A high risk registry to find congenital deafness Otolaryngol Clin North Am 4 1971 369 399
3. DA Campbell DP McHale KA Brown LM Moynihan M Houseman G Karbani G Parry A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22 J Med Genet 34 1997 1015 1017
4. N Chiannilkulchai P Pasturaud I Richard C Auffray JS Beckmann A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene Hum Mol Genet 4 1995 717 725
5. MM Cohen RJ Gorlin Epidemiology, etiology, and genetic patterns RJ Gorlin HV Toriello MM Cohen Hereditary hearing loss and its syndromes 1995 Oxford University Press Oxford 9 21
6. I del Castillo M Villamar M Sarduy L Romero C Herraiz FJ Hernández M Rodríguez A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22 Hum Mol Genet 5 1996 1383 1387
7. C Dib S Fauré C Fizames D Samson N Drouot A Vignal P Millasseau A comprehensive genetic map of the human genome based on 5,264 microsatellites Nature 380 1996 152 154
8. F Fougerousse O Broux I Richard V Allamand A Pereira de Souza N Bourg L Brenguier Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy Hum Mol Genet 3 1994 285 293
9. GM Lathrop JM Lalouel C Julier J Ott Multilocus linkage analysis in humans: detection of linkage and estimation of recombination Am J Hum Genet 37 1985 482 498
10. WP Robinson B Horsthemke S Leonard S Malcolm C Morton RD Nicholls RJ Ritchie Report of the Third International Workshop on Human Chromosomal 15 Mapping 1996 Cytogenet Cell Genet 76 1997 1 13
11. G Van Camp PJ Willems RJH Smith Nonsyndromic hearing impairment: unparalleled heterogeneity Am J Hum Genet 60 1997 758 764