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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 |
2008-4-17
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pubmed:abstractText |
To determine the incidence of classical 21-hydroxylase deficiency (21-OHD) in Estonia from 1978 to 2004, and describe their phenotype and genotype.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1423-0046
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pubmed:author |
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pubmed:copyrightInfo |
(c) 2008 S. Karger AG, Basel
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pubmed:issnType |
Electronic
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pubmed:volume |
69
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
227-32
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pubmed:meshHeading |
pubmed-meshheading:18204270-Adrenal Hyperplasia, Congenital,
pubmed-meshheading:18204270-Alleles,
pubmed-meshheading:18204270-Child,
pubmed-meshheading:18204270-Child, Preschool,
pubmed-meshheading:18204270-Estonia,
pubmed-meshheading:18204270-European Continental Ancestry Group,
pubmed-meshheading:18204270-Female,
pubmed-meshheading:18204270-Genotype,
pubmed-meshheading:18204270-Humans,
pubmed-meshheading:18204270-Incidence,
pubmed-meshheading:18204270-Infant,
pubmed-meshheading:18204270-Infant, Newborn,
pubmed-meshheading:18204270-Male,
pubmed-meshheading:18204270-Metabolism, Inborn Errors,
pubmed-meshheading:18204270-Neonatal Screening,
pubmed-meshheading:18204270-Phenotype,
pubmed-meshheading:18204270-Sex Ratio,
pubmed-meshheading:18204270-Steroid 21-Hydroxylase
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pubmed:year |
2008
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pubmed:articleTitle |
Incidence of classical 21-hydroxylase deficiency and distribution of CYP21A2 mutations in Estonia.
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pubmed:affiliation |
Department of Paediatrics, University of Tartu, Tartu, Estonia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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