Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions
- Author
- EICHLER, E. E1 ; HAMMOND, H. A1 ; MACPHERSON, J. N; WARD, P. A1 ; NELSON, D. L1
[1] Baylor coll. medicine, human genome cent., dep. molecular human genetics, Houston TX 77030, United States - Source
Human molecular genetics (Print). 1995, Vol 4, Num 12, pp 2199-2208 ; ref : 25 ref
- Publisher
- Oxford University Press, Oxford
- Publication country
- United Kingdom
- Document type
- Article
- Language
- English
- Keyword (fr)
- DNA microsatellite Délétion Ethnie Facteur risque Fréquence génique Gène Génétique population Homme Instabilité Polymorphisme Prédisposition Stabilité X fragile syndrome Fragilité chromosomique
- Keyword (en)
- Microsatellite DNA Deletion Ethnic group Risk factor Gene frequency Gene Population genetics Human Instability Polymorphism Predisposition Stability Fragile X syndrome Chromosome fragility
- Keyword (es)
- DNA microsatélite Deleción Etnia Factor riesgo Frecuencia génica Gen Genética población Hombre Inestabilidad Polimorfismo Predisposición Estabilidad X frágil síndrome Fragilidad cromosómica
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B23 Medical genetics / 002B23C Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)
- Discipline
- Medical genetics
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2932147
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
10.1093/hmg/4.12.2199 
https://dx.doi.org/10.1093/hmg/4.12.2199
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