Yellow nail syndrome: with familiar primary hypoplasia of lymphatics, manifest late in life.
Identifieur interne : 011274 ( Main/Exploration ); précédent : 011273; suivant : 011275Yellow nail syndrome: with familiar primary hypoplasia of lymphatics, manifest late in life.
Auteurs : G. C. WellsSource :
- Proceedings of the Royal Society of Medicine [ 0035-9157 ] ; 1966.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Lymphoedème, Troubles de la pigmentation.
- Adulte d'âge moyen, Humains, Mâle, Ongles.
English descriptors
- KwdEn :
- MESH :
- genetics : Lymphedema, Pigmentation Disorders.
- Humans, Male, Middle Aged, Nails.
Url:
PubMed: 5933133
PubMed Central: 1900882
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Pmc, to step Corpus: 001A35
- to stream Pmc, to step Curation: 001A34
- to stream Pmc, to step Checkpoint: 004910
- to stream PubMed, to step Corpus: 007C75
- to stream PubMed, to step Curation: 007C75
- to stream PubMed, to step Checkpoint: 007C75
- to stream Ncbi, to step Merge: 00A807
- to stream Ncbi, to step Curation: 00A807
- to stream Ncbi, to step Checkpoint: 00A807
- to stream Main, to step Merge: 012394
- to stream Main, to step Curation: 011274
Le document en format XML
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<term>Pigmentation Disorders (genetics)</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term>
<term>Humains</term>
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<term>Mâle</term>
<term>Ongles</term>
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