𝔖 Bobbio Scriptorium
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Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screening

✍ Scribed by K Sarafoglou; C P Lorentz; N Otten; W S Oetting; S K G Grebe


Book ID
115091954
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
508 KB
Volume
82
Category
Article
ISSN
0009-9163

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