LymphedemaV1, Istex, Curation, bibRecord, 001C41

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype

Identifieur interne : 001C41 ( Istex/Curation ); précédent : 001C40; suivant : 001C42

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype

Auteurs : J. Tarleton [États-Unis] ; A. Kenneson [États-Unis] ; A K Taylor [États-Unis] ; K. Crandall [États-Unis] ; R. Fletcher [États-Unis] ; R. Casey [États-Unis] ; P S Hart [États-Unis] ; D. Hatton [États-Unis] ; G. Fisch [États-Unis] ; S T Warren [États-Unis]

Source :

Journal of Medical Genetics [ 0022-2593 ] ; 2002-03.

RBID : ISTEX:3E0EE21C9984F1D065CB03D673D6DF666C211EA7

English descriptors

KwdEn :
- CGG repeat, FMR1, fragile X syndrome.

Url:

https://api.istex.fr/document/3E0EE21C9984F1D065CB03D673D6DF666C211EA7/fulltext/pdf

DOI: 10.1136/jmg.39.3.196

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ISTEX:3E0EE21C9984F1D065CB03D673D6DF666C211EA7

Le document en format XML

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<country xml:lang="fr">États-Unis</country>
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<country xml:lang="fr">États-Unis</country>
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A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype

Source :

English descriptors

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri