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Q33334349-9F252DC8-3859-4CB0-B9F4-908DFF865940
Q33334349-9F252DC8-3859-4CB0-B9F4-908DFF865940
BestRank
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http://www.wikidata.org/entity/statement/Q33334349-9F252DC8-3859-4CB0-B9F4-908DFF865940
High frequency of copy number variations and sequence variants at CYP21A2 locus: implication for the genetic diagnosis of 21-hydroxylase deficiency.
P2860
Q33334349-9F252DC8-3859-4CB0-B9F4-908DFF865940
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33334349-9F252DC8-3859-4CB0-B9F4-908DFF865940
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type
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Statement
wasDerivedFrom
4fd05ed292320f4ba47a56339c87e351b762fa3e
P2860
Benefits of neonatal screening for congenital adrenal hyperplasia (21-hydroxylase deficiency) in Sweden.