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2 research outputs found
Feingold syndrome associated with two novel **MYCN** mutations in sporadic and familial cases including monozygotic twins
Author
Blaumeiser Bettina
Borozdin Wiktor
Kohlhase J\ufcrgen
Oehl-Jaschkowitz Barbara
Publication venue
Publication date
01/01/2008
Field of study
Full text link
Institutional Repository Universiteit Antwerpen
Five patients with novel overlapping interstitial deletions in 8q22.2q22.3
Author
Buysse Karen
Clayton-Smith Jill
+9Â more
David Albert
Engels Hartmut
Kohlhase J\ufcrgen
Kuechler Alm
Le Caignec C\ue9dric
Mari Francesca
Mortier Geert
Renieri Alessandra
Wieczorek Dagmar
Publication venue
Publication date
01/01/2011
Field of study
Full text link
Institutional Repository Universiteit Antwerpen
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