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A novel mutation in theMSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomaly

✍ Scribed by Michella Ghassibé; Vincent Bernier; Laurence M. Boon; Miikka Vikkula

Publisher
Springer
Year
2006
Tongue
English
Weight
109 KB
Volume
165
Category
Article
ISSN
0340-6997

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