Homozygous Mutation in Synaptic Vesicle Glycoprotein 2A Gene Results in Intractable Epilepsy, Involuntary Movements, Microcephaly, and Developmental and Growth Retardation by Serajee, Fatema J., MBBS, Huq, Ahm M., MD

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Posterior Reversible Encephalopathy and Cerebral Vasoconstriction in a Patient With Hemolytic Uremic Syndrome by Agarwal, Rajkumar, MD, Davis, Cresha, MD, Altinok, Deniz, MD, Serajee, Fatema J., MBBS

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O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling by Selvan, Nithya, George, Stephan, Serajee, Fatema J., Shaw, Marie, Hobson, Lynne, Kalscheuer, Vera, Prasad, Nripesh, Levy, Shawn E., Taylor, Juliet, Aftimos, Salim, Schwartz, Charles E., Huq, Ahm M., Gecz, Jozef, Wells, Lance

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Carbamazepine responsive episodic dystonia and hallucination due to pyruvate dehydrogenase E2 (DLAT) gene mutation by Policherla, Jasmine, Serajee, Fatema J, Rashid, Salman, Huq, A H M Mahbubul

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Association of Reelin gene polymorphisms with autism by Serajee, Fatema J., Zhong, Hailang, Mahbubul Huq, A.H.M.

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Association of Y Chromosome Haplotypes With Autism by Serajee, Fatema J., Mahbubul Huq, A.H.M.

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Polymorphisms in Xenobiotic Metabolism Genes and Autism by Serajee, Fatema J., Nabi, Rafiqun, Hailang Zhong, Mahbubul Huq, A.H.M.

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Association of tryptophan 2,3 dioxygenase gene polymorphism with autism by Nabi, Rafiqun, Serajee, Fatema J., Chugani, Diane C., Zhong, Hailang, Huq, A.H.M. Mahbubul

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Homozygous Myotonic Dystrophy With Craniosynostosis by Cerghet, Mirela, Tapos, Daniela, Serajee, Fatema J., Mahbubul Huq, A. H. M.

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No association between single nucleotide polymorphisms in DLX6 and piccolo genes at 7q21-q22 and autism by Nabi, Rafiqun, Zhong, Hailang, Serajee, Fatema J, Huq, AHM Mahbubul

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