Noonan syndrome associated congenital hypertrophic cardiomyopathy and the role of sarcomere gene mutations von Joshi, V.A, Roberts, A.E, Kucherlapati, R.S

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Insertion of DNA sequences into the human chromosomal β-globin locus by homologous recombination von Smithies, Oliver, Gregg, Ronald G., Boggs, Sallie S., Koralewski, Michael A., Kucherlapati, Raju S.

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Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan syndrome von Tartaglia, M, Mehler, E.L, Goldberg, R, Zampino, G, Brunner, H.G, Kremer, H, van der Burgt, I, Crosby, A.H, Ion, A, Jeffery, S, Kalidas, K, Patton, M.A, Kucherlapati, R.S, Gelb, B

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Homologous Recombination between Plasmids in Mammalian Cells can be Enhanced by Treatment of Input DNA von Kucherlapati, Raju S., Eves, Eva M., Song, Kyu-Young, Morse, Brian S., Smithies, Oliver

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Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14–q15 breakpoint regio... von Fejzo, Marlena Schoenberg, Yoon, Sung-Joo, Montgomery, Kate T., Rein, Mitchell S., Weremowicz, Stanislawa, Krauter, Kenneth S., Dorman, Thomas E., Fletcher, Jonathan A., Mao, Jen-I, Moir, Donald T., Kucherlapati, Raju S., Morton, Cynthia C.

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Correction: Mutations in the protein tyrosine kinase gene, PTPN11, cause Noonan syndrome von Tartaglia, M., Mehler, E.L., Goldberg, R., Zampino, G., Brunner, H.G., Kremer, H., van der Burgt, I., Crosby, A.H., Ion, A., Jeffery, S., Kalidas, K., Patton, M.A., Kucherlapati, R.S., Gelb, B.

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Generation of a Nested Series of Interstitial Deletions in Yeast Artificial Chromosomes Carrying Human DNA von Campbell, Colin, Gulati, Rajiv, Nandi, Asit K., Floy, Kimberly, Hieter, Philip, Kucherlapati, Raju S.

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Detection of interspecific translocations in mouse-human hybrids by alkaline Giemsa staining von Friend, K.K., Dorman, B.P., Kucherlapati, R.S., Ruddle, F.H.

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A physical map of the human genome von McPherson, J D, Marra, M, Hillier, L, Waterston, R H, Chinwalla, A, Wallis, J, Sekhon, M, Wylie, K, Mardis, E R, Wilson, R K, Fulton, R, Kucaba, T A, Wagner-McPherson, C, Barbazuk, W B, Gregory, S G, Humphray, S J, French, L, Evans, R S, Bethel, G, Whittaker, A, Holden, J L, McCann, O T, Dunham, A, Soderlund, C, Scott, C E, Bentley, D R, Schuler, G, Chen, H C, Jang, W, Green, E D, Idol, J R, Maduro, V V, Montgomery, K T, Lee, E, Miller, A, Emerling, S, Kucherlapati, Gibbs, R, Scherer, S, Gorrell, J H, Sodergren, E, Clerc-Blankenburg, K, Tabor, P, Naylor, S, Garcia, D, de Jong, P J, Catanese, J J, Nowak, N, Osoegawa, K, Qin, S, Rowen, L, Madan, A, Dors, M, Hood, L, Trask, B, Friedman, C, Massa, H, Cheung, V G, Kirsch, I R, Reid, T, Yonescu, R, Weissenbach, J, Bruls, T, Heilig, R, Branscomb, E, Olsen, A, Doggett, N, Cheng, J F, Hawkins, T, Myers, R M, Shang, J, Ramirez, L, Schmutz, J, Velasquez, O, Dixon, K, Stone, N E, Cox, D R, Haussler, D, Kent, W J, Furey, T, Rogic, S, Kennedy, S, Jones, S, Rosenthal, A, Wen, G, Schilhabel, M, Gloeckner, G, Nyakatura, G, Siebert, R, Schlegelberger, B, Korenberg, J, Chen, X N, Fujiyama, A, Hattori, M, Toyoda, A, Yada, T, Park, H S, Sakaki, Y, Shimizu, N, Asakawa, S

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Introduction and expression of a fetal human globin gene in mouse fibroblasts von Hsiung, N, Roginski, R S, Henthorn, P, Smithies, O, Kucherlapati, R, Skoultchi, A I

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