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A Case of 3β-Hydroxysteroid Dehydrogenase Type II (HSD3B2) Deficiency Picked up by Neonatal Screening for 21-Hydroxylase Deficiency: Difficulties and Delay in Etiologic Diagnosis

✍ Scribed by Nordenström, Anna ;Forest, Maguelone G. ;Wedell, Anna


Book ID
119984760
Publisher
S. Karger AG
Year
2007
Tongue
English
Weight
135 KB
Volume
68
Category
Article
ISSN
1663-2818

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