LymphedemaV1, France, Analysis, bibRecord, 000501

Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri‐dimensional ultrasonography

Identifieur interne : 000501 ( France/Analysis ); précédent : 000500; suivant : 000502

Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri‐dimensional ultrasonography

Auteurs : Jean-Marc Levaillant [France] ; Marion Gérard-Blanluet [France] ; Muriel Holder-Espinasse [France] ; Anne-Sylvie Valat-Rigot [France] ; Louise Devisme [France] ; Hélène Cavé [France] ; Sylvie Manouvrier-Hanu [France]

Source :

Prenatal Diagnosis [ 0197-3851 ] ; 2006-04.

RBID : ISTEX:33886773A3A6649A787BA490176BB706E45FDD21

Abstract

Prenatal diagnosis of multiple congenital anomalies is difficult, and usually molecular biology cannot immediately confirm the suspected syndrome. Fetal dysmorphology is useful tool in the diagnosis process, with limitations.

Url:

https://api.istex.fr/document/33886773A3A6649A787BA490176BB706E45FDD21/fulltext/pdf

DOI: 10.1002/pd.1412

Affiliations:

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

to stream Istex, to step Corpus: 001774
to stream Istex, to step Curation: 001774
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to stream Main, to step Exploration: 007B70
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ISTEX:33886773A3A6649A787BA490176BB706E45FDD21

Le document en format XML

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<author><name sortKey="Gerard Lanluet, Marion" sort="Gerard Lanluet, Marion" uniqKey="Gerard Lanluet M" first="Marion" last="Gérard-Blanluet">Marion Gérard-Blanluet</name>
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<author><name sortKey="Holder Spinasse, Muriel" sort="Holder Spinasse, Muriel" uniqKey="Holder Spinasse M" first="Muriel" last="Holder-Espinasse">Muriel Holder-Espinasse</name>
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<author><name sortKey="Valat Igot, Anne Ylvie" sort="Valat Igot, Anne Ylvie" uniqKey="Valat Igot A" first="Anne-Sylvie" last="Valat-Rigot">Anne-Sylvie Valat-Rigot</name>
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<author><name sortKey="Devisme, Louise" sort="Devisme, Louise" uniqKey="Devisme L" first="Louise" last="Devisme">Louise Devisme</name>
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<author><name sortKey="Cave, Helene" sort="Cave, Helene" uniqKey="Cave H" first="Hélène" last="Cavé">Hélène Cavé</name>
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<author><name sortKey="Manouvrier Anu, Sylvie" sort="Manouvrier Anu, Sylvie" uniqKey="Manouvrier Anu S" first="Sylvie" last="Manouvrier-Hanu">Sylvie Manouvrier-Hanu</name>
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<name sortKey="Manouvrier Anu, Sylvie" sort="Manouvrier Anu, Sylvie" uniqKey="Manouvrier Anu S" first="Sylvie" last="Manouvrier-Hanu">Sylvie Manouvrier-Hanu</name>
<name sortKey="Valat Igot, Anne Ylvie" sort="Valat Igot, Anne Ylvie" uniqKey="Valat Igot A" first="Anne-Sylvie" last="Valat-Rigot">Anne-Sylvie Valat-Rigot</name>
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Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri‐dimensional ultrasonography

Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri‐dimensional ultrasonography

Source :

Abstract

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

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Le document en format XML

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Pour mettre un lien sur cette page dans le réseau Wicri