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Intrauterine therapy of goitrous hypothyroidism in a boy with a new compound heterozygous mutation (Y453D and C800R) in the thyroid peroxidase gene. A long-term follow-up

✍ Scribed by Kirsten Börgel; Joachim Pohlenz; Wolfgang Holzgreve; Jurgen H. Bramswig


Book ID
113429128
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
102 KB
Volume
193
Category
Article
ISSN
1097-6868

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