A Novel Autosomal Recessive Non-Syndromic Deafness Locus, <i>DFNB66</i>, Maps to Chromosome 6p21.2-22.3 in a Large Tunisian Consanguineous Family-Reference-Cited by-同舟云学术

A Novel Autosomal Recessive Non-Syndromic Deafness Locus, DFNB66, Maps to Chromosome 6p21.2-22.3 in a Large Tunisian Consanguineous Family

Published:2005 Issue:3 Volume:60 Page:123-128
ISSN:0001-5652
Container-title:Human Heredity
language:en
Short-container-title:Hum Hered

Author:

Tlili Abdelaziz,Männikkö Minna,Charfedine Ilhem,Lahmar Imed,Benzina Zeineb,Ben Amor Mohamed,Driss Nabil,Ala-Kokko Leena,Drira Mohamed,Masmoudi Saber,Ayadi Hammadi

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics

Reference19 articles.

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2. Cohen MM, Gorlin RJ: Epidemiology, etiology and genetic patterns; in: Gorlin RJ, Toriello HV, Cohen MM (eds): Hereditary Hearing Loss and Its Syndromes. Oxford: Oxford University Press, 1995, pp 9-21.

3. Gorlin RJ: Genetic hearing loss with no associated abnormalities; in Gorlin RJ, Toriello HV, Cohen MM (eds): Hereditary Hearing Loss and Its Syndromes. Oxford, Oxford University Press, 1995, pp 43-61.

4. A comprehensive genetic map of the human genome based on 5,264 microsatellites

5. Extensive Polymorphism of a (CA)n Microsatellite Located in the HLA-DQA1/DQB1 Class II Region

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