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Association of hyperprolinaemia type I and heparin cofactor II deficiency with CATCH 22 syndrome: evidence for a contiguous gene syndrome locating the proline oxidase gene

✍ Scribed by J. Jaeken; N. Goemans; J. -P. Fryns; I. François; F. de Zegher


Book ID
105312339
Publisher
Springer
Year
1996
Tongue
English
Weight
241 KB
Volume
19
Category
Article
ISSN
0141-8955

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