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Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome

✍ Scribed by Dufke, A.; Seidel, J.; Schöning, M.; Döbler-Neumann, M.; Kelbova, C.; Liehr, T.; Beensen, V.; Backsch, C.; Klein-Vogler, U.; Enders, H.


Book ID
120551298
Publisher
S. Karger AG
Year
2000
Tongue
French
Weight
160 KB
Volume
91
Category
Article
ISSN
1424-8581

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## Abstract ## BACKGROUND Wolf‐Hirschhorn syndrome (WHS) is a well‐known genetic condition characterized by typical facial anomalies, midline defects, skeletal anomalies, prenatal and postnatal growth retardation, hypotonia, mental retardation, and seizures. Affected patients with a microdeletion

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