LymphedemaV1, PubMed, Checkpoint, bibRecord, 004C83

Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.

Identifieur interne : 004C83 ( PubMed/Checkpoint ); précédent : 004C82; suivant : 004C84

Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.

Auteurs : J P Fryns

Source :

American journal of medical genetics [ 0148-7299 ] ; 1995.

RBID : pubmed:7545871

Descripteurs français

KwdFr :
- Chromosomes humains de la paire 13, Délétion de segment de chromosome, Enfant d'âge préscolaire, Humains, Incapacités de développement (génétique), Lymphoedème (génétique), Malformations des cloisons cardiaques (génétique), Malformations multiples (génétique), Microcéphalie (génétique), Mâle, Syndrome.
MESH :
- génétique : Incapacités de développement, Lymphoedème, Malformations des cloisons cardiaques, Malformations multiples, Microcéphalie.
- Chromosomes humains de la paire 13, Délétion de segment de chromosome, Enfant d'âge préscolaire, Humains, Mâle, Syndrome.

English descriptors

KwdEn :
- Abnormalities, Multiple (genetics), Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 13, Developmental Disabilities (genetics), Heart Septal Defects (genetics), Humans, Lymphedema (genetics), Male, Microcephaly (genetics), Syndrome.
MESH :
- genetics : Abnormalities, Multiple, Developmental Disabilities, Heart Septal Defects, Lymphedema, Microcephaly.
- Child, Preschool, Chromosome Deletion, Chromosomes, Human, Pair 13, Humans, Male, Syndrome.

DOI: 10.1002/ajmg.1320570332
PubMed: 7545871

Affiliations:

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to stream PubMed, to step Corpus: 005367
to stream PubMed, to step Curation: 005367

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pubmed:7545871

Le document en format XML

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<term>Developmental Disabilities (genetics)</term>
<term>Heart Septal Defects (genetics)</term>
<term>Humans</term>
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<term>Syndrome</term>
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<term>Délétion de segment de chromosome</term>
<term>Enfant d'âge préscolaire</term>
<term>Humains</term>
<term>Incapacités de développement (génétique)</term>
<term>Lymphoedème (génétique)</term>
<term>Malformations des cloisons cardiaques (génétique)</term>
<term>Malformations multiples (génétique)</term>
<term>Microcéphalie (génétique)</term>
<term>Mâle</term>
<term>Syndrome</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Abnormalities, Multiple</term>
<term>Developmental Disabilities</term>
<term>Heart Septal Defects</term>
<term>Lymphedema</term>
<term>Microcephaly</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Incapacités de développement</term>
<term>Lymphoedème</term>
<term>Malformations des cloisons cardiaques</term>
<term>Malformations multiples</term>
<term>Microcéphalie</term>
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<keywords scheme="MESH" xml:lang="en"><term>Child, Preschool</term>
<term>Chromosome Deletion</term>
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<term>Humans</term>
<term>Male</term>
<term>Syndrome</term>
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<term>Délétion de segment de chromosome</term>
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<DateRevised><Year>2004</Year>
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<Title>American journal of medical genetics</Title>
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	Serveur d'exploration sur le lymphœdème
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Serveur d'exploration sur le lymphœdème

Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.

Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.

Source :

Descripteurs français

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

Pour générer des pages wiki