Homozygous Mutation of the FGFR1 Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex Development

2016 ◽  
Vol 10 (1) ◽  
pp. 16-22 ◽  
Author(s):  
Inas Mazen ◽  
Heba Amin ◽  
Alaa Kamel ◽  
Mona El Ruby ◽  
Joelle Bignon-Topalovic ◽  
...  
Keyword(s):  
Congenital Heart Disease ◽  
Heart Disease ◽  
Congenital Heart ◽  
Homozygous Mutation ◽  
Disorder Of Sex Development ◽  
Sex Development
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