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Nabil N Moghrabi

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2009
Validation of Fanconi anemia complementation Group A assignment using molecular analysisNabil N Moghrabi, Monique A Johnson, Marvin J Yoshitomi, et al.
Human Mutation|June 19, 2019
Homozygous loss-of-function variants of TASP1, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomaliesJehan Suleiman, Korbinian M Riedhammer, Timothy Jicinsky, et al.
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Showing results (1-10 of 2) with videos related to

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Pageof 1
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2009
Validation of Fanconi anemia complementation Group A assignment using molecular analysisNabil N Moghrabi, Monique A Johnson, Marvin J Yoshitomi, et al.
Human Mutation|June 19, 2019
Homozygous loss-of-function variants of TASP1, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomaliesJehan Suleiman, Korbinian M Riedhammer, Timothy Jicinsky, et al.
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