Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis
von Koskull, H.; Leisti, J.
Duodecim; Laaketieteellinen Aikakauskirja 108(17): 1445-1447
1992
ISSN/ISBN: 0012-7183 PMID: 1366164 Document Number: 398870
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