Serveur d'exploration sur la visibilité du Havre

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Very low alpha‐fetoprotein in Down syndrome maternal serum screening

Identifieur interne : 001471 ( Main/Exploration ); précédent : 001470; suivant : 001472

Very low alpha‐fetoprotein in Down syndrome maternal serum screening

Auteurs : Françoise Muller [France] ; Sophie Dreux [France] ; Corinne Sault [France] ; Armelle Galland [France] ; Hugues Puissant [France] ; Gisèle Couplet [France] ; Catherine Lemay [France] ; Marie-Estelle Larcher [France] ; Gilles Renom [France]

Source :

RBID : ISTEX:B2E15B0E2EA568BB99033F70F9A4317B8F53664C

English descriptors

Abstract

To establish the frequency of very low maternal serum AFP and to differentiate congenital AFP deficiency from those diseases known to be associated with low AFP.

Url:
DOI: 10.1002/pd.646


Affiliations:


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


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Very low alpha‐fetoprotein in Down syndrome maternal serum screening</title>
<author>
<name sortKey="Muller, Francoise" sort="Muller, Francoise" uniqKey="Muller F" first="Françoise" last="Muller">Françoise Muller</name>
</author>
<author>
<name sortKey="Dreux, Sophie" sort="Dreux, Sophie" uniqKey="Dreux S" first="Sophie" last="Dreux">Sophie Dreux</name>
</author>
<author>
<name sortKey="Sault, Corinne" sort="Sault, Corinne" uniqKey="Sault C" first="Corinne" last="Sault">Corinne Sault</name>
</author>
<author>
<name sortKey="Galland, Armelle" sort="Galland, Armelle" uniqKey="Galland A" first="Armelle" last="Galland">Armelle Galland</name>
</author>
<author>
<name sortKey="Puissant, Hugues" sort="Puissant, Hugues" uniqKey="Puissant H" first="Hugues" last="Puissant">Hugues Puissant</name>
</author>
<author>
<name sortKey="Couplet, Gisele" sort="Couplet, Gisele" uniqKey="Couplet G" first="Gisèle" last="Couplet">Gisèle Couplet</name>
</author>
<author>
<name sortKey="Lemay, Catherine" sort="Lemay, Catherine" uniqKey="Lemay C" first="Catherine" last="Lemay">Catherine Lemay</name>
</author>
<author>
<name sortKey="Larcher, Marie Stelle" sort="Larcher, Marie Stelle" uniqKey="Larcher M" first="Marie-Estelle" last="Larcher">Marie-Estelle Larcher</name>
</author>
<author>
<name sortKey="Renom, Gilles" sort="Renom, Gilles" uniqKey="Renom G" first="Gilles" last="Renom">Gilles Renom</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:B2E15B0E2EA568BB99033F70F9A4317B8F53664C</idno>
<date when="2003" year="2003">2003</date>
<idno type="doi">10.1002/pd.646</idno>
<idno type="url">https://api.istex.fr/document/B2E15B0E2EA568BB99033F70F9A4317B8F53664C/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000E00</idno>
<idno type="wicri:Area/Istex/Curation">000E00</idno>
<idno type="wicri:Area/Istex/Checkpoint">000656</idno>
<idno type="wicri:doubleKey">0197-3851:2003:Muller F:very:low:alpha</idno>
<idno type="wicri:Area/Main/Merge">001507</idno>
<idno type="wicri:Area/Main/Curation">001471</idno>
<idno type="wicri:Area/Main/Exploration">001471</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">Very low alpha‐fetoprotein in Down syndrome maternal serum screening</title>
<author>
<name sortKey="Muller, Francoise" sort="Muller, Francoise" uniqKey="Muller F" first="Françoise" last="Muller">Françoise Muller</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Service de Biochimie, Hôpital Ambroise Paré, Boulogne</wicri:regionArea>
<wicri:noRegion>Boulogne</wicri:noRegion>
<wicri:noRegion>Boulogne</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Dreux, Sophie" sort="Dreux, Sophie" uniqKey="Dreux S" first="Sophie" last="Dreux">Sophie Dreux</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Service de Biochimie, Hôpital Ambroise Paré, Boulogne</wicri:regionArea>
<wicri:noRegion>Boulogne</wicri:noRegion>
<wicri:noRegion>Boulogne</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Sault, Corinne" sort="Sault, Corinne" uniqKey="Sault C" first="Corinne" last="Sault">Corinne Sault</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire Marcel Mérieux, Lyon</wicri:regionArea>
<placeName>
<settlement type="city">Lyon</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Galland, Armelle" sort="Galland, Armelle" uniqKey="Galland A" first="Armelle" last="Galland">Armelle Galland</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire Marcel Mérieux, Lyon</wicri:regionArea>
<placeName>
<settlement type="city">Lyon</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Puissant, Hugues" sort="Puissant, Hugues" uniqKey="Puissant H" first="Hugues" last="Puissant">Hugues Puissant</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Génétique, CHU Angers</wicri:regionArea>
<wicri:noRegion>CHU Angers</wicri:noRegion>
<wicri:noRegion>CHU Angers</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Couplet, Gisele" sort="Couplet, Gisele" uniqKey="Couplet G" first="Gisèle" last="Couplet">Gisèle Couplet</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire Biolille, Lille</wicri:regionArea>
<placeName>
<settlement type="city">Lille</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Lemay, Catherine" sort="Lemay, Catherine" uniqKey="Lemay C" first="Catherine" last="Lemay">Catherine Lemay</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Biologie Endocrinienne et Osseuse, CHU Amiens</wicri:regionArea>
<wicri:noRegion>CHU Amiens</wicri:noRegion>
<wicri:noRegion>CHU Amiens</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Larcher, Marie Stelle" sort="Larcher, Marie Stelle" uniqKey="Larcher M" first="Marie-Estelle" last="Larcher">Marie-Estelle Larcher</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Laboratoire Stahl‐Kuntzel, Metz</wicri:regionArea>
<placeName>
<settlement type="city">Metz</settlement>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Renom, Gilles" sort="Renom, Gilles" uniqKey="Renom G" first="Gilles" last="Renom">Gilles Renom</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Biochimie, Hôpital Calmette, CHRU Lille</wicri:regionArea>
<wicri:noRegion>CHRU Lille</wicri:noRegion>
<wicri:noRegion>CHRU Lille</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Prenatal Diagnosis</title>
<title level="j" type="abbrev">Prenat. Diagn.</title>
<idno type="ISSN">0197-3851</idno>
<idno type="eISSN">1097-0223</idno>
<imprint>
<publisher>John Wiley & Sons, Ltd.</publisher>
<pubPlace>Chichester, UK</pubPlace>
<date type="published" when="2003-07">2003-07</date>
<biblScope unit="volume">23</biblScope>
<biblScope unit="issue">7</biblScope>
<biblScope unit="page" from="584">584</biblScope>
<biblScope unit="page" to="587">587</biblScope>
</imprint>
<idno type="ISSN">0197-3851</idno>
</series>
<idno type="istex">B2E15B0E2EA568BB99033F70F9A4317B8F53664C</idno>
<idno type="DOI">10.1002/pd.646</idno>
<idno type="ArticleID">PD646</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0197-3851</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>AFP</term>
<term>Down syndrome screening</term>
<term>congenital deficiency</term>
<term>maternal serum markers</term>
<term>prenatal diagnosis</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract">To establish the frequency of very low maternal serum AFP and to differentiate congenital AFP deficiency from those diseases known to be associated with low AFP.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>France</li>
</country>
<settlement>
<li>Lille</li>
<li>Lyon</li>
<li>Metz</li>
</settlement>
</list>
<tree>
<country name="France">
<noRegion>
<name sortKey="Muller, Francoise" sort="Muller, Francoise" uniqKey="Muller F" first="Françoise" last="Muller">Françoise Muller</name>
</noRegion>
<name sortKey="Couplet, Gisele" sort="Couplet, Gisele" uniqKey="Couplet G" first="Gisèle" last="Couplet">Gisèle Couplet</name>
<name sortKey="Dreux, Sophie" sort="Dreux, Sophie" uniqKey="Dreux S" first="Sophie" last="Dreux">Sophie Dreux</name>
<name sortKey="Galland, Armelle" sort="Galland, Armelle" uniqKey="Galland A" first="Armelle" last="Galland">Armelle Galland</name>
<name sortKey="Larcher, Marie Stelle" sort="Larcher, Marie Stelle" uniqKey="Larcher M" first="Marie-Estelle" last="Larcher">Marie-Estelle Larcher</name>
<name sortKey="Lemay, Catherine" sort="Lemay, Catherine" uniqKey="Lemay C" first="Catherine" last="Lemay">Catherine Lemay</name>
<name sortKey="Puissant, Hugues" sort="Puissant, Hugues" uniqKey="Puissant H" first="Hugues" last="Puissant">Hugues Puissant</name>
<name sortKey="Renom, Gilles" sort="Renom, Gilles" uniqKey="Renom G" first="Gilles" last="Renom">Gilles Renom</name>
<name sortKey="Sault, Corinne" sort="Sault, Corinne" uniqKey="Sault C" first="Corinne" last="Sault">Corinne Sault</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/France/explor/LeHavreV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001471 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001471 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/France
   |area=    LeHavreV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:B2E15B0E2EA568BB99033F70F9A4317B8F53664C
   |texte=   Very low alpha‐fetoprotein in Down syndrome maternal serum screening
}}

Wicri

This area was generated with Dilib version V0.6.25.
Data generation: Sat Dec 3 14:37:02 2016. Site generation: Tue Mar 5 08:25:07 2024