Homozygous deletion of six olfactory receptor genes in a subset of individuals with Beta-thalassemia. by Jessica Van Ziffle, Wendy Yang, Farid F Chehab

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First report of a deletion encompassing an entire exon in the homogentisate 1,2-dioxygenase gene causing alkaptonuria. by Mohammad Zouheir Habbal, Tarek Bou-Assi, Jun Zhu, Renius Owen, Farid F Chehab

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Effects of FoxO4 overexpression on cholesterol biosynthesis, triacylglycerol accumulation, and glucose uptake by Jun Zhu, Khalid Mounzih, Eric F. Chehab, Nico Mitro, Enrique Saez, Farid F. Chehab

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Correction: Duplication of , and in an Obese Female with a t(7;22)(q32.1;q11.2) Chromosomal Translocation and Clinical Features Resembling Coffin-Siris Syndrome. by Jun Zhu, Jun Qiu, Gregg Magrane, Malak Abedalthagafi, Andrea Zanko, Mahin Golabi, Farid F. Chehab

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Duplication of C7orf58, WNT16 and FAM3C in an obese female with a t(7;22)(q32.1;q11.2) chromosomal translocation and clinical features resembling Coffin-Siris Syndrome. by Jun Zhu, Jun Qiu, Gregg Magrane, Malak Abedalthagafi, Andrea Zanko, Mahin Golabi, Farid F Chehab

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A systematic review of high impact CpG sites and regions for MGMT methylation in glioblastoma [A systematic review of MGMT methylation in GBM] by David Gibson, Anh Huan Vo, Hannah Lambing, Prithanjan Bhattacharya, Peggy Tahir, Farid F. Chehab, Nicholas Butowski

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Genome-wide DNA methylation is predictive of outcome in juvenile myelomonocytic leukemia by Elliot Stieglitz, Tali Mazor, Adam B. Olshen, Huimin Geng, Laura C. Gelston, Jon Akutagawa, Daniel B. Lipka, Christoph Plass, Christian Flotho, Farid F. Chehab, Benjamin S. Braun, Joseph F. Costello, Mignon L. Loh

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