A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A

Dina Fine, Hagit Flusser, Barak Markus, Zamir Shorer, Libe Gradstein, Shareef Khateeb, Yshia Langer, Ginat Narkis, Ruth Birk, Aharon Galil,

European Journal of Human Genetics · 2014 · 22 citations · 8 references

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