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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
Daniela Larizza, Mariaclara Cuccia, Miryam Martinetti, Mohamad Maghnie, Elisabetta Dondi, Laura Salvaneschi, Francesca SeveriVolume:
40
Year:
1994
Language:
english
Pages:
7
DOI:
10.1111/j.1365-2265.1994.tb02441.x
File:
PDF, 592 KB
english, 1994