Human Genome Epidemiology Literature Finder
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Query Trace: Syndrome and FRMD4A[original query] |
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A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A. European journal of human genetics : EJHG 2014 Nov . Fine Dina, Flusser Hagit, Markus Barak, Shorer Zamir, Gradstein Libe, Khateeb Shareef, Langer Yshia, Narkis Ginat, Birk Ruth, Galil Aharon, Shelef Ilan, Birk Ohad |
- Page last reviewed:Feb 1, 2024
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