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Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency

✍ Scribed by E. Mornet; P. Couillin; F. Kutten; M. C. Raux; P. C. White; D. Cohen; A. Boué; J. Dausset


Publisher
Springer
Year
1986
Tongue
English
Weight
1019 KB
Volume
74
Category
Article
ISSN
0340-6717

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