The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase von Attree, Olivier, Olivos, Isabelle M, Okabe, Ichiro, Bailey, L. Charles, Nelson, David L, Lewis, Richard A, Mclnnes, Roderick R, Nussbaum, Robert L

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Lowe Syndrome, a deficiency of a phosphatidyl-inositol 4,5-bisphosphate 5-phosphatase in the Golgi apparatus von Suchy, Sharon F., Olivos-Glander, Isabelle M., Nussbaum, Robert L.

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Ocrl1, a PtdIns(4,5)P2 5-Phosphatase, Is Localized to the Trans-Golgi Network of Fibroblasts and Epithelial Cells von Dressman, Marlene Armitage, Olivos-Glander, Isabelle M, Nussbaum, Robert L, Suchy, Sharon F

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The oculocerebrorenal syndrome gene product is a 105-kD protein localized to the Golgi complex von OLIVOS-GLANDER, I. M, JÄNNE, P. A, NUSSBAUM, R. L

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Construction and characterization of a yeast artificial chromosome library for Xpter-Xq27.3: A systematic determination of cocloning rate and X-chromosome representation von Lee, Jeannie T., Murgia, Alessandra, Sosnoski, Donna M., Olivos, Isabelle M., Nussbaum, Robert L.

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Ocrl1, a PtdIns(4,5)P 2 5-Phosphatase, Is Localized to the Trans -Golgi Network of Fibroblasts and Epithelial Cells von Dressman, Marlene Armitage, Olivos-Glander, Isabelle M., Nussbaum, Robert L., Suchy, Sharon F.

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Omega-3 Fatty Acid Supplementation During Pregnancy and Respiratory Symptoms in Children von Escamilla-Nuñez, María Consuelo, MSc, Barraza-Villarreal, Albino, PhD, Hernández-Cadena, Leticia, PhD, Navarro-Olivos, Efraín, MD, Sly, Peter D., MBBS, MD, DSc, Romieu, Isabelle, MD, MPH, ScD

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Medical comorbidities in bipolar disorder (BIPCOM): clinical validation of risk factors and biomarkers to improve prevention and treatment. Study protocol von de Girolamo, Giovanni, Andreassen, Ole A., Bauer, Michael, Brambilla, Paolo, Calza, Stefano, Citerà, Nicholas, Corcoy, Rosa, Fagiolini, Andrea, Garcia-Argibay, Miguel, Godin, Ophélia, Klingler, Florian, Kobayashi, Nene F., Larsson, Henrik, Leboyer, Marion, Matura, Silke, Martinelli, Alessandra, De la Peña-Arteaga, Víctor, Poli, Roberto, Reif, Andreas, Ritter, Philipp, Rødevand, Linn N., Magno, Marta, Caselani, Elisa

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Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome von Johnston, Jennifer J., Olivos-Glander, Isabelle, Turner, Joyce, Aleck, Kyrieckos, Bird, Lynne M., Mehta, Lakshmi, Schimke, R. Neil, Heilstedt, Heidi, Spence, J. Edward, Blancato, Jan, Biesecker, Leslie G.

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Recurrent cutaneous infections, hyperkeratosis, ichthyosis and deafness and a newly identified connexin 26 gene mutation A40V von Montgomery, Jay R, Martin, Bryan L, Olivos-Glander, Isabelle, Turner, Marie, Darnell, Dirk, Holland, Steven M

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Molecular and clinical analyses of greig cephalopolysyndactyly and pallister-hall syndromes : Robust phenotype prediction from the type and position of GL13 mutations von JOHNSTON, Jennifer J, OLIVOS-GLANDER, Isabelle, BOOTH, Carol, CURRY, Cynthia J, DAVID, Albert, DINULOS, Mary Beth, FLANNERY, David B, FOX, Michelle A, GRAHAM, John M, GRANGE, Dorothy K, GUTTMACHER, Alan E, HANNIBAL, Mark C, KILLORAN, Christina, HENN, Wolfram, HENNEKAM, Raoul C. M, HOLMES, Lewis B, EUGENE HOYME, H, LEPPIG, Kathleen A, LIN, Angela E, MACLEOD, Patrick, MANCHESTER, David K, MARCELIS, Carlo, MAZZANTI, Laura, ELSON, Emma, MCCANN, Emma, MCDONALD, Marie T, MENDELSOHN, Nancy J, MOESCHLER, John B, MOGHADDAM, Billur, NERI, Giovanni, NEWBURY-ECOB, Ruth, PAGON, Roberta A, PHILLIPS, John A, SADLER, Laurie S, TURNER, Joyce T, STOLER, Joan M, TILSTRA, David, WALSH VOCKLEY, Catherine M, ZACKAI, Elaine H, ZADEH, Touran M, BRUETON, Louise, BLACK, Graeme Charles M, BIESECKER, Leslie G, PETERS, Kathryn F, ABBOTT, Margaret H, AUGHTON, David J, AYLSWORTH, Arthur S, BAMSHAD, Michael J

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