Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.
Identifieur interne : 004C83 ( PubMed/Checkpoint ); précédent : 004C82; suivant : 004C84Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.
Auteurs : J P FrynsSource :
- American journal of medical genetics [ 0148-7299 ] ; 1995.
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 :
English descriptors
- KwdEn :
- MESH :
DOI: 10.1002/ajmg.1320570332
PubMed: 7545871
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
pubmed:7545871Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Abnormalities, Multiple (genetics)</term>
<term>Child, Preschool</term>
<term>Chromosome Deletion</term>
<term>Chromosomes, Human, Pair 13</term>
<term>Developmental Disabilities (genetics)</term>
<term>Heart Septal Defects (genetics)</term>
<term>Humans</term>
<term>Lymphedema (genetics)</term>
<term>Male</term>
<term>Microcephaly (genetics)</term>
<term>Syndrome</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Chromosomes humains de la paire 13</term>
<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>
</keywords>
<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>
</keywords>
<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>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Child, Preschool</term>
<term>Chromosome Deletion</term>
<term>Chromosomes, Human, Pair 13</term>
<term>Humans</term>
<term>Male</term>
<term>Syndrome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Chromosomes humains de la paire 13</term>
<term>Délétion de segment de chromosome</term>
<term>Enfant d'âge préscolaire</term>
<term>Humains</term>
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<DateRevised><Year>2004</Year>
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<Title>American journal of medical genetics</Title>
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<ArticleTitle>Microcephaly/lymphedema and terminal deletion of the long arm of chromosome 13.</ArticleTitle>
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