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Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families

✍ Scribed by Daniela Larizza; Mariaclara Cuccia; Miryam Martinetti; Mohamad Maghnie; Elisabetta Dondi; Laura Salvaneschi; Francesca Severi


Book ID
114719865
Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
592 KB
Volume
40
Category
Article
ISSN
0300-0664

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