Crystal unit von LAIRD ARTHUR G

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Magnetic field detector von SLONCZEWSKI THADDEUS, LAIRD ARTHUR G

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Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis von Wapner, Ronald J, Martin, Christa Lese, Levy, Brynn, Ballif, Blake C, Eng, Christine M, Zachary, Julia M, Savage, Melissa, Platt, Lawrence D, Saltzman, Daniel, Grobman, William A, Klugman, Susan, Scholl, Thomas, Simpson, Joe Leigh, McCall, Kimberly, Aggarwal, Vimla S, Bunke, Brian, Nahum, Odelia, Patel, Ankita, Lamb, Allen N, Thom, Elizabeth A, Beaudet, Arthur L, Ledbetter, David H, Shaffer, Lisa G, Jackson, Laird

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Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies von Miller, David T., Adam, Margaret P., Aradhya, Swaroop, Biesecker, Leslie G., Brothman, Arthur R., Carter, Nigel P., Church, Deanna M., Crolla, John A., Eichler, Evan E., Epstein, Charles J., Faucett, W. Andrew, Feuk, Lars, Friedman, Jan M., Hamosh, Ada, Jackson, Laird, Kaminsky, Erin B., Kok, Klaas, Krantz, Ian D., Kuhn, Robert M., Lee, Charles, Ostell, James M., Rosenberg, Carla, Scherer, Stephen W., Spinner, Nancy B., Stavropoulos, Dimitri J., Tepperberg, James H., Thorland, Erik C., Vermeesch, Joris R., Waggoner, Darrel J., Watson, Michael S., Martin, Christa Lese, Ledbetter, David H.

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Assessing Attention Deficit Hyperactivity Disorder via Quantitative Electroencephalography: An Initial Validation Study von Monastra, Vincent J, Lubar, Joel F, Linden, Michael, VanDeusen, Peter, Green, George, Wing, William, Phillips, Arthur, Fenger, T. Nick

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Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B von Krantz, Ian D, McCallum, Jennifer, DeScipio, Cheryl, Kaur, Maninder, Gillis, Lynette A, Yaeger, Dinah, Jukofsky, Lori, Wasserman, Nora, Bottani, Armand, Morris, Colleen A, Nowaczyk, Malgorzata J M, Toriello, Helga, Bamshad, Michael J, Carey, John C, Rappaport, Eric, Kawauchi, Shimako, Lander, Arthur D, Calof, Anne L, Li, Hui-hua, Devoto, Marcella, Jackson, Laird G

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Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays von Bi, Weimin, Breman, Amy, Shaw, Chad A, Stankiewicz, Pawel, Gambin, Tomasz, Lu, Xinyan, Cheung, Sau Wai, Jackson, Laird G, Lupski, James R, Van den Veyver, Ignatia B, Beaudet, Arthur L

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Detection of ≥1 Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays von Bi, Weimin, Breman, Amy, Shaw, Chad A., Stankiewicz, Pawel, Gambin, Tomasz, Lu, Xinyan, Cheung, Sau Wai, Jackson, Laird G., Lupski, James R., den Veyver, Ignatia B. Van, Beaudet, Arthur L.

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Chromosomal Microarray Versus Karyotyping for Prenatal Diagnosis von Wapner, Ronald J, Martin, Christa Lese, Levy, Brynn, Ballif, Blake C, Eng, Christine M, Zachary, Julia M, Savage, Melissa, Platt, Lawrence D, Saltzman, Daniel, Grobman, William A, Klugman, Susan, Scholl, Thomas, Simpson, Joe Leigh, McCall, Kimberly, Aggarwal, Vimla S, Bunke, Brian, Nahum, Odelia, Patel, Ankita, Lamb, Allen N, Thom, Elizabeth A, Beaudet, Arthur L, Ledbetter, David H, Shaffer, Lisa G, Jackson, Laird

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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies von Miller, David T, Adam, Margaret P, Aradhya, Swaroop, Biesecker, Leslie G, Brothman, Arthur R, Carter, Nigel P, Church, Deanna M, Crolla, John A, Eichler, Evan E, Epstein, Charles J, Faucett, W. Andrew, Feuk, Lars, Friedman, Jan M, Hamosh, Ada, Jackson, Laird, Kaminsky, Erin B, Kok, Klaas, Krantz, Ian D, Kuhn, Robert M, Lee, Charles, Ostell, James M, Rosenberg, Carla, Scherer, Stephen W, Spinner, Nancy B, Stavropoulos, Dimitri J, Tepperberg, James H, Thorland, Erik C, Vermeesch, Joris, Waggoner, Darrel J, Watson, Michael S, Martin, Christa Lese, Ledbetter, David H

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Hepatic protein kinase C: Translocation stimulated by prolactin and partial hepatectomy von Buckley, Arthur R., Putnam, Charles W., Evans, Ronald, Laird, Hugh E., Shah, Gul N., Montgomery, David W., Russell, Diane Haddock

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Group B streptococcal endocarditis detected by echocardiography von Weinberg, Arthur G., Laird, W. Pennock

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SPONTANEOUS REVERSION AT THE HPRT LOCUS IN CELLS FROM A PATIENT WITH A MILD VARIANT OF THE LESCH-NYHAN SYNDROME von Aylsworth, Arthur S, Jackson, Laird G, Kredich, Nicholas M

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Fatal Haemophilus influenzae endocarditis diagnosed by echocardiography in an infant von Laird, W P, Nelson, J D, Weinberg, A G, Huffines, F D

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Hemodynamic evaluation of intra-aortic balloon pumping in man von Buckley, M J, Leinbach, R C, Kastor, J A, Laird, J D, Kantrowitz, A R, Madras, P N, Sanders, C A, Austen, W G

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Dimethylacetamide: A Hitherto Unrecognized Hallucinogenic Agent von Weiss, Arthur J., Mancall, Elliott L., Koltes, John A., White, Joseph C., Jackson, Laird G.

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Chemotherapy by intralymphatic infusion von Jackson, Laird G., Wallace, Sidney, Weiss, Arthur

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Chemotherapy in Ovarian Malignancy: Tumor Sensitivity Testing von RIGGS, JOSEPH A., JACKSON, LAIRD G., WEISS, ARTHUR J., FARELL, DAVID M., TRAIMAN, RICHARD

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PROFESSIONAL REGISTRATION von Fanning, Oliver M., Barton, Arthur G., Laird, Edward H., Merrill, Vincent N., Packard, Marion V., Sanders, Spencer E., Schaffer, Otto G., Webel, Richard K.

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PROFESSIONAL REGISTRATION von Huntington, George C., Andrews, Wolcott E., Brooks, James H., Churchill, Richard, Hoffmann, Arthur F., Laird, Edward H., Linnard, Lawrence G., Myers, Russell W., Park, Neil Hamill

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