[Association of aplasia cutis congenita with coarctation of the aorta: a coincidence?].
Identifieur interne : 001122 ( France/Analysis ); précédent : 001121; suivant : 001123[Association of aplasia cutis congenita with coarctation of the aorta: a coincidence?].
Auteurs : H. Bruel [France] ; J. Poinsot ; J P Chabrolle ; V. LayetSource :
- Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [ 0929-693X ] ; 1999.
English descriptors
- KwdEn :
- MESH :
- complications : Aortic Coarctation, Ectodermal Dysplasia.
- genetics : Aortic Coarctation, Ectodermal Dysplasia.
- pathology : Aortic Coarctation, Ectodermal Dysplasia.
- Female, Genetic Predisposition to Disease, Humans, Infant, Newborn.
Abstract
The association of aplasia cutis congenita and aortic coarctation could be a coincidence.
PubMed: 10587744
Affiliations:
Links toward previous steps (curation, corpus...)
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- to stream PubMed, to step Curation: 000402
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- to stream Ncbi, to step Merge: 000008
- to stream Ncbi, to step Curation: 000008
- to stream Ncbi, to step Checkpoint: 000008
- to stream Main, to step Merge: 001A58
- to stream Main, to step Curation: 001A10
- to stream Main, to step Exploration: 001A10
- to stream France, to step Extraction: 001122
Links to Exploration step
pubmed:10587744Le document en format XML
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