Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals von Koenig, M., Hoffman, E.P., Bertelson, C.J., Monaco, A.P., Feener, C., Kunkel, L.M.

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Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene von Monaco, Anthony P., Neve, Rachael L., Colletti-Feener, Chris, Bertelson, Corlee J., Kurnit, David M., Kunkel, Louis M.

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Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment von Monaco, Anthony P., Bertelson, Corlee J., Middlesworth, William, Colletti, Chris-Anne, Aldridge, John, Fischbeck, Kenneth H., Bartlett, Richard, Pericak-Vance, Margaret A., Roses, Allen D., Kunkel, Louis M.

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Localization of the McLeod locus (XK) within XP21 by deletion analysis von BERTELSON, C. J, POGO, A. O, CHAUDHURI, A, MARSH, W. L, REDMAN, C. M, BANERJEE, D, SYMMANS, W. A, SIMON, T, FREY, D, KUNKEL, L. M

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An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus von Monaco, Anthony P., Bertelson, Corlee J., Liechti-Gallati, Sabina, Moser, Hans, Kunkel, Louis M.

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Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy von MONACO, A. P, BERTELSON, C. J, COLLETTI-FEENER, C, KUNKEL, L. M

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Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families von Bertelson, C J, Bartley, J A, Monaco, A P, Colletti-Feener, C, Fischbeck, K, Kunkel, L M

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Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy von Fischbeck, K H, Ritter, A W, Tirschwell, D L, Kunkel, L M, Bertelson, C J, Monaco, A P, Hejtmancik, J F, Boehm, C, Ionasescu, V, Ionasescu, R

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RECOMBINATION WITH PERT87 (DXS164) IN FAMILIES WITH X-LINKED MUSCULAR DYSTROPHY von Fischbeck, K.H, Ritter, A.W, Tirschwell, D.L, Kunkel, L.M, Bertelson, C.J, Monaco, A.P, Hejtmancik, J.F, Boehm, C, Ionasescu, V, Ionasescu, R, Pericak-Vance, M, Kandt, R, Roses, A.D

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Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD in normal and affected individuals von KOENIG, M, HOFFMAN, E. P, BERTELSON, C. J, MONACO, A. P, FEENER, C, KUNKEL, L. M

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Localization of the McLeod locus (XK) XP21 by deletion analysis von Bertelson, C J, Pogo, A O, Chaudhuri, A, Marsh, W L, Redman, C M, Banerjee, D, Symmans, WA, Simon, T, Frey, D, Kunkel, L M

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Associations of Sex, Race, and Apolipoprotein E Alleles With Multiple Domains of Cognition Among Older Adults von Walters, Skylar, Contreras, Alex G, Eissman, Jaclyn M, Mukherjee, Shubhabrata, Lee, Michael L, Choi, Seo-Eun, Scollard, Phoebe, Trittschuh, Emily H, Mez, Jesse B, Bush, William S, Kunkle, Brian W, Naj, Adam C, Peterson, Amalia, Gifford, Katherine A, Cuccaro, Michael L, Cruchaga, Carlos, Pericak-Vance, Margaret A, Farrer, Lindsay A, Wang, Li-San, Haines, Jonathan L, Jefferson, Angela L, Kukull, Walter A, Keene, C. Dirk, Saykin, Andrew J, Thompson, Paul M, Martin, Eden R, Bennett, David A, Barnes, Lisa L, Schneider, Julie A, Crane, Paul K, Hohman, Timothy J, Dumitrescu, Logan

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Whole genome‐wide sequence analysis of long‐lived families (Long‐Life Family Study) identifies MTUS2 gene associated with late‐onset Alzheimer's disease von Vardarajan, Badri, Andersen, Stacy L., Thyagarajan, Bharat, Yashin, Anatoli, Krinsky‐McHale, Sharon, Handen, Benjamin L., Schupf, Nicole, Lee, Joseph H., Barral, Sandra, Bell, Karen, Bulova, Peter, Cohen, Ann D., Constantino, John N., Handen, Benjamin L., Head, Elizabeth, Honig, Lawrence, Ikonomovic, Milos D., Keator, David, Lao, Patrick, Lott, Ira T., Mapstone, Mark, Parisi, Melissa, Pulsifer, Margaret, Varadarajan, Badri, Zaman, Shahid, Adams, Perrie M., Allen, Mariet, Atwood, Craig S., Ayres, Gayle, Barral, Sandra, Beecham, Gary W., Biber, Sarah A., Boeve, Bradley F., Bush, William S., Byrd, Goldie, Chan, Kwun C., Chen, Yen‐Chi, Chesselet, Marie‐Francoise, Chin, Nathaniel A., Cranney, Marissa, Cruchaga, Carlos, DeToledo, John C., Ertekin‐Taner, Nilufer, Faber, Kelley M., Fallin, Daniele, Farrer, Lindsay A., Galasko, Douglas R., Gefen, Tamar, Goate, Alison M., Grabowski, Thomas, Haines, Jonathan L., Hakonarson, Hakon, Hall, Kathleen, Hall, James R., Harari, Oscar, Honig, Lawrence S., Hyman, Bradley T., Hynan, Linda, Johnson, Kimberly, Jun, Gyungah, Kamboh, M. Ilyas, Khaleeq, Aisha, Kunkle, Brian W., LaFerla, Frank M., Lah, James J., Lieberman, Andrew P., Lipton, Richard B., Lopez, Oscar L., Marquez, David, Marson, Daniel C., Masurkar, Arjun V., Mukherjee, Shubhabrata, Nudelman, Kelley, Parisi, Joseph E., Pavlik, Valory, Perez, Victoria, Petersen, Ronald C., Polk, Marsha, Qu, Liming, Quiceno, Mary, Raj, Ashok, Rajabli, Farid, Roberson, Erik D., Royall, Donald R., Sano, Mary, Song, Yeunjoo, George‐Hyslop, Peter St, Stern, Robert A., Stevens, Alan, Sultzer, David, Valladares, Otto, Van Deerlin, Vivianna M., Vance, Jeffery M., Vassar, Robert, Welsh‐Bohmer, Kathleen A., Wilms, Henrick, Wisniewski, Thomas, Woon, Martin, Younkin, Steven G., Zhu, Congcong

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Blood-based protein predictors of dementia severity as measured by δ: Replication across biofluids and cohorts von Royall, Donald R., Bishnoi, Ram J., Palmer, Raymond F., Pavlik, Valory, Massman, Paul, Darby, Eveleen, Rodriguear, Monica, Ansari, Aisha Khaleeq, DeToledo, John C., Reddy, Hemachandra, Wilms, Henrick, Johnson, Kim, Perez, Victoria, Fairchild, Thomas, Knebl, Janice, O'Bryant, Sid E., Hall, James R., Johnson, Leigh, Barber, Robert C., Mains, Douglas, Alvarez, Lisa, Cullum, Munro, Rosenberg, Roger, Williams, Benjamin, Quiceno, Mary, Reisch, Joan, Hynan, Linda S., Huebinger, Ryan, Smith, Janet, Nguyen, Trung, Royall, Donald, Palmer, Raymond, Polk, Marsha, Stevens, Alan, Ory, Marcia, Paydarfar, David, Bertelson, John, Woon, Martin, Ayres, Gayle, Aguirre, Alyssa, Wilhelmsen, Kirk C., Tilson, Jeffrey L.

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Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy von Kunkel, Louis M.

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Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: Isolation and use of J66 (DXS268), a distal intragenic marker von van Ommen, G.J.B., Bertelson, C., Ginjaar, H.B., den Dunnen, J.T, Bakker, E., Chelly, J., Matton, M., van Essen, A.J., Bartley, J., Kunkel, L.M., Pearson, P.L.

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Spatial constraints on attention to speech in the blind von Bertelson, Paul, Morais, José, Mousty, Philippe, Hublet, Claude

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CASKET ASSEMBLY von BERTELSON, PETER C, PIKOR, STEVEN J, BETHUNE, WILLIAM, LEPAGE, BERNARD E

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MODES OPÉRATOIRES DANS LA LECTURE DE L'ÉCRITURE BRAILLE von Bertelson, P., Mousty, Ph

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Un effet résiduel dans l'enchainement de réactions de choix von Bertelson, P.

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