Publications by authors named "Shareef Khateeb"

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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

Eur J Hum Genet· December 2015

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Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutation.
Miora Feinstein, Barak Markus, Iris Noyman, Hannah Shalev, Hagit Flusser, Shareef Khateeb

Am J Hum Genet· December 2010

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Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9.
Ortal Barel, Stavit A Shalev, Rivka Ofir, Asi Cohen, Joel Zlotogora, Shareef Khateeb

Am J Hum Genet· August 2008

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PLA2G6 mutation underlies infantile neuroaxonal dystrophy.
Shareef Khateeb, Hagit Flusser, Rivka Ofir, Ilan Shelef, Ginat Narkis

Am J Hum Genet· November 2006

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