Genetics of microtia and associated syndromes
- Author
- ALASTI, F1 2 ; VAN CAMP, G1
[1] Department of Medical Genetics, University of Antwerp, Antwerp, Belgium
[2] Department of Molecular Genetics, National Institute for Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran, Islamic Republic of - Source
Journal of medical genetics. 2009, Vol 46, Num 6, pp 361-369, 9 p ; ref : 133 ref
- Publisher
- BMJ Publishing Group, London
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- Aplasie Génétique Homme Maladie héréditaire Microtie Pavillon oreille Syndrome complexe Malformation
- Keyword (en)
- Aplasia Genetics Human Genetic disease Microtia Pinna Complex syndrome Malformation
- Keyword (es)
- Aplasia Genética Hombre Enfermedad hereditaria Microtia Pabellón auricular Síndrome complejo Malformación
- Classification
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A04 Molecular and cellular biology
- Pascal
- 002 Biological and medical sciences / 002A Fundamental and applied biological sciences. Psychology / 002A07 Genetics of eukaryotes. Biological and molecular evolution
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23A General aspects. Genetic counseling
- Discipline
- Eukaryotes genetics. Biological and molecular evolution Medical genetics Molecular and cell biology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 21568030
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
10.1136/jmg.2008.062158 
https://dx.doi.org/10.1136/jmg.2008.062158
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