Academic Interests:

Genetics of autism and mental retardation, craniofacial anomalies, dysmorphology, and prenatal genetics

Selected Publications:

Abdul-Rahman OA, La TH, Kwan A, Schlaubitz S, Barsh GS, Enns GM, and Hudgins L. Genitopatellar syndrome: Expanding the phenotype and excluding mutations in LMX1B and TBX4. Am J Med Genet [in press], 2006.

Abdul-Rahman OA and Hudgins L. The diagnostic utility of a genetics evaluation in children with pervasive developmental disorders. Genet Med 8(1):50-54, 2006.

Cushman LJ, Torres-Martinez W, Cherry AM, Manning MA, Abdul-Rahman O, Anderson CE, Punnett HH, Thurston VC, Sweeney D, Vance GH. A report of three patients with an interstitial deletion of 15q24. Am J Med Genet 137(1); 65-71, 2005.

Abdul-Rahman OA, Gay H, Caldwell E, Megason GC. Cryptococcal sepsis diagnosed by bone marrow examination. J Pediat Hem Oncol 26(8): 526-528, 2004.