Publications by authors named "Mustafa Shafiq"

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Deletion 1q43 encompassing only CHRM3 in a patient with autistic disorder.
Andrea Klunder Petersen, Ausaf Ahmad, Mustafa Shafiq, Brigette Brown-Kipphut, Chin-To Fong

Eur J Med Genet· February 2013

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A 0.7 Mb de novo duplication at 7q21.3 including the genes DLX5 and DLX6 in a patient with split-hand/split-foot malformation.
Milen Velinov, Ausaf Ahmad, Brigette Brown-Kipphut, Mustafa Shafiq, Jonathan Blau

Am J Med Genet A· December 2012

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