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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

CODEN
CLGNAY
ISSN
0009-9163
Scientific domain
Genetics
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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