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Congenital primary hypothyroidism with subsequent adenomatous goiter in a Turkish patient caused by a homozygous 10-bp deletion in the thyroid peroxidase (TPO) gene

✍ Scribed by Nicole Pfarr; Thomas J. Musholt; Petra B. Musholt; Rita Brzezinska; Joachim Pohlenz


Book ID
108703398
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
183 KB
Volume
64
Category
Article
ISSN
0300-0664

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