LymphedemaV1, France, Analysis, bibRecord, 000663

FOXL2 mutation screening in a large panel of POF patients and XX males

Identifieur interne : 000663 ( France/Analysis ); précédent : 000662; suivant : 000664

FOXL2 mutation screening in a large panel of POF patients and XX males

Auteurs : E. De Baere [Belgique] ; B. Lemercier [France] ; S. Christin-Maitre [France] ; D. Durval [Brésil] ; L. Messiaen [Belgique] ; M. Fellous [France] ; R. Veitia [France]

Source :

Journal of Medical Genetics [ 0022-2593 ] ; 2002-08.

RBID : ISTEX:8998DF1A03E12751D647479B85DFECA08F4B748B

English descriptors

KwdEn :
- BPES, blepharophimosis-ptosis-epicanthus inversus syndrome, FOXL2, PIS, polled intersex syndrome, POF, premature ovarian failure, XX sex reversal, blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), polled intersex syndrome (PIS), premature ovarian failure (POF).

Url:

DOI: 10.1136/jmg.39.8.e43

Affiliations:

Links to Exploration step

ISTEX:8998DF1A03E12751D647479B85DFECA08F4B748B

Le document en format XML

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<term>XX sex reversal</term>
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{{Explor lien
   |wiki=    Wicri/Sante
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   |texte=   FOXL2 mutation screening in a large panel of POF patients and XX males
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Serveur d'exploration sur le lymphœdème

FOXL2 mutation screening in a large panel of POF patients and XX males

FOXL2 mutation screening in a large panel of POF patients and XX males

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

	Serveur d'exploration sur le lymphœdème
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