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Q33635253-CD6969EC-89BD-4906-9CCB-C12F259BE138
Q33635253-CD6969EC-89BD-4906-9CCB-C12F259BE138
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Statement
http://www.wikidata.org/entity/statement/Q33635253-CD6969EC-89BD-4906-9CCB-C12F259BE138
Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center
P2860
Q33635253-CD6969EC-89BD-4906-9CCB-C12F259BE138
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33635253-CD6969EC-89BD-4906-9CCB-C12F259BE138
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wasDerivedFrom
396d0b92b8e99c373f1cd732d5f3f921764772b7
P2860
High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.