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GENATLAS PHENOTYPE

last update : 25-02-2009

Symbol	BGS2
Location	7p21.1
Name	Baller-Gerold syndrome 2
Corresponding gene	TWIST1
Main clinical features	craniosynostosis with radial defects
Genetic determination	autosomal recessive
Function/system disorder
Type	disease

Remark(s)

possible clinical overlap with Saethre-Chotzen syndrome (Seto,01)