Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation von Battaglia, Agatino, Hoyme, H. Eugene, Dallapiccola, Bruno, Zackai, Elaine, Hudgins, Louanne, McDonald-McGinn, Donna, Bahi-Buisson, Nadia, Romano, Corrado, Williams, Charles A, Brailey, Lisa L, Zuberi, Sameer M, Carey, John C

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Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene von Yamaguchi, Saori, Brailey, Lisa L., Morizono, Hiroki, Bale, Allen E., Tuchman, Mendel

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Cardiac and CNS defects in a mouse with targeted disruption of suppressor of fused von Cooper, Ayanna F, Yu, Kuan Ping, Brueckner, Martina, Brailey, Lisa L, Johnson, Linda, McGrath, James M, Bale, Allen E

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Integrin-mediated signaling regulates AP-1 transcription factors and proliferation in osteoblasts von Cowles, Elizabeth A., Brailey, Lisa L., Gronowicz, Gloria A.

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Aspiration in patients with acute stroke von Daniels, Stephanie K., Brailey, Kevin, Priestly, Daniel H., Herrington, Lisa R., Weisberg, Leon A., Foundas, Anne L.

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Apheresis and the Thrombotic Thrombocytopenic Purpura Syndrome: Current Advances in Diagnosis, Pathophysiology, and Management von Brailey, Lisa Louise, Brecher, Mark E., Bandarenko, Nicholas

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