The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23
- Author
- ALI, G1 ; SANTOS, R. L. P2 ; JOHN, P1 ; WAMBANGCO, M. A. L2 ; LEE, K2 ; AHMAD, W1 ; LEAL, S. M2
[1] Department of Biological Sciences, Quaid-I-Azam University, Islamabad, Pakistan
[2] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States - Source
Clinical genetics. 2006, Vol 69, Num 5, pp 429-433, 5 p ; ref : 25 ref
- Publisher
- Blackwell, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Author keyword
- 12p13.2-p11.23 DFNB62 Pakistan autosomal recessive non-syndromic hearing impairment
- Keyword (fr)
- Caractère autosomique Caractère récessif Carte génétique Chromosome Génétique Homme Maladie héréditaire Trouble audition Pakistan ORL pathologie Asie
- Keyword (en)
- Autosomal character Recessive character Genetic mapping Chromosome Genetics Human Genetic disease Auditory disorder Pakistan ENT disease Asia
- Keyword (es)
- Carácter autosómico Carácter recesivo Mapa genético Cromosoma Genética Hombre Enfermedad hereditaria Trastorno auditivo Pakistan ORL patología Asia
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23A General aspects. Genetic counseling
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 17729424
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1111/j.1399-0004.2006.00611.x 
https://dx.doi.org/10.1111/j.1399-0004.2006.00611.x
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