A novel autosomal dominant non-syndromic deafness locus (DFNA48) maps to 12q13-q14 in a large Italian family

Author:

D'Adamo Pio,Pinna Maura,Capobianco Saverio,Cesarani Antonio,D'Eustacchio Angela,Fogu Pina,Carella Massimo,Seri Marco,Gasparini Paolo

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference5 articles.

1. Camp G van, Willems PJ, Smith RJH (1997) Nonsyndromic hearing impairment: unparalleled heterogeneity. Am J Hum Genet 60:758–764

2. Cottingham RW, Idury RM, Shaffer AA (1993) Faster sequential genetic linkage computations. Am J Hum Genet 53:252–263

3. Lathrop GM, Lalouel JM, Julier C, Ott J (1984) Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 81:3443–3446

4. Mukhopadhyay N, Almsay L, Schroeder M, Mulvihill WP, Weeks DE (1999) Mega2, a data-handling program for facilitating genetic linkage and association analyses. Am J Hum Genet 65:abstract no. 436

5. Sobel E, Lange K (1996) Descent graphs in pedigree analysis: application to haplotyping, location scores, and marker sharing statistics. Am J Hum Genet 58:1323–1337

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