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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2002-4-9
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|
pubmed:abstractText |
To report the clinical features of the loose anagen hair syndrome and to test the hypothesis that the typical gap between the hair and the inner root sheath may result from hereditary defects in the inner root sheath or the apposed companion layer.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
|
|
pubmed:status |
MEDLINE
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|
pubmed:month |
Apr
|
|
pubmed:issn |
0003-987X
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|
pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
138
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
501-6
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|
pubmed:dateRevised |
2008-3-17
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|
pubmed:meshHeading |
|
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pubmed:year |
2002
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|
pubmed:articleTitle |
Is the loose anagen hair syndrome a keratin disorder? A clinical and molecular study.
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|
pubmed:affiliation |
Unité de Dermatologie Pédiatrique, Hôpital Pellegrin-Enfants, Bordeaux, France.
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pubmed:publicationType |
Journal Article
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