Genetic predisposition to human disease: allele-specific expression and low-penetrance regulatory loci von de la Chapelle, A

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The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia von Eisfeld, A-K, Mrózek, K, Kohlschmidt, J, Nicolet, D, Orwick, S, Walker, C J, Kroll, K W, Blachly, J S, Carroll, A J, Kolitz, J E, Powell, B L, Wang, E S, Stone, R M, de la Chapelle, A, Byrd, J C, Bloomfield, C D

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Mutations in the CCND1 and CCND2 genes are frequent events in adult patients with t(8;21)(q22;q22) acute myeloid leukemia von Eisfeld, A-K, Kohlschmidt, J, Schwind, S, Nicolet, D, Blachly, J S, Orwick, S, Shah, C, Bainazar, M, Kroll, K W, Walker, C J, Carroll, A J, Powell, B L, Stone, R M, Kolitz, J E, Baer, M R, de la Chapelle, A, Mrózek, K, Byrd, J C, Bloomfield, C D

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Adult acute myeloid leukemia with trisomy 11 as the sole abnormality is characterized by the presence of five distinct gene mutations: MLL-PTD, DNMT3A, U2AF1, FLT3-ITD and IDH2 von Eisfeld, A-K, Kohlschmidt, J, Mrózek, K, Blachly, J S, Nicolet, D, Kroll, K, Orwick, S, Carroll, A J, Stone, R M, de la Chapelle, A, Byrd, J C, Bloomfield, C D

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No evidence for microsatellite instability in acute myeloid leukemia von Walker, C J, Eisfeld, A-K, Genutis, L K, Bainazar, M, Kohlschmidt, J, Mrózek, K, Carroll, A J, Kolitz, J E, Powell, B L, Wang, E S, Stone, R M, Bundschuh, R, de la Chapelle, A, Bloomfield, C D

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A diagnostic biochip for the comprehensive analysis of MLL translocations in acute leukemia von MAROC, N, MOREL, A, FERT, V, HERMITTE, F, BEILLARD, E, DE LA CHAPELLE, A. L, FUND, X, MOZZICONACCI, M-J, DUPONT, M, CAYUELA, J-M, GABERT, J, KOKI, A

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A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome von Clendenning, M, Senter, L, Hampel, H, Robinson, K Lagerstedt, Sun, S, Buchanan, D, Walsh, M D, Nilbert, M, Green, J, Potter, J, Lindblom, A, de la Chapelle, A

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MicroRNA-related sequence variations in human cancers von Wojcicka, A., de la Chapelle, A., Jazdzewski, K.

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A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24 von HUILING HE, NAGY, Rebecca, LIYANARACHCHI, Sandya, HONG JIAO, WEI LI, SUSTER, Saul, KERE, Juha, DE LA CHAPELLE, Albert

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The Frequency of Muir-Torre Syndrome Among Lynch Syndrome Families von South, Christopher D., Hampel, Heather, Comeras, Ilene, Westman, Judith A., Frankel, Wendy L., de la Chapelle, Albert

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Genetic susceptibility to non-polyposis colorectal cancer von Lynch, Henry T, de la Chapelle, Albert

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GENETIC TESTING FOR CANCER PREDISPOSITION von Eng, Charis, Hampel, Heather, Chapelle, Albert de la

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The genetic basis of colorectal cancer in a population-based incident cohort with a high rate of familial disease von Woods, M O, Younghusband, H B, Parfrey, P S, Gallinger, S, McLaughlin, J, Dicks, E, Stuckless, S, Pollett, A, Bapat, B, Mrkonjic, M, de la Chapelle, A, Clendenning, M, Thibodeau, S N, Simms, M, Dohey, A, Williams, P, Robb, D, Searle, C, Green, J S, Green, R C

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Reconstructing hominid Y evolution : X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through line-line recombination von SCHWARTZ, A, CHAN, D. C, BROWN, L. G, ALAGAPPAN, R, PETTAY, D, DISTECHE, C, MCGILLIVRAY, B, DE LA CHAPELLE, A, PAGE, D. C

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Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC gene von Nagy, R, Wang, H, Albrecht, B, Wieczorek, D, Gillessen- Kaesbach, G, Haan, E, Meinecke, P, de la Chapelle, A, Westman, JA

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Long-range PCR facilitates the identification of PMS2-specific mutations von Clendenning, Mark, Hampel, Heather, LaJeunesse, Jennifer, Lindblom, Annika, Lockman, Jan, Nilbert, Mef, Senter, Leigha, Sotamaa, Kaisa, de la Chapelle, Albert

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Recurrent and founder mutations in the PMS2 gene von Tomsic, J, Senter, L, Liyanarachchi, S, Clendenning, M, Vaughn, C P, Jenkins, M A, Hopper, J L, Young, J, Samowitz, W, de la Chapelle, A

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Genetic predisposition to colorectal cancer von de la Chapelle, Albert

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Disease gene mapping in isolated human populations: the example of Finland von de la Chapelle, A

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Amnionless (AMN) mutations in Imerslund–Gräsbeck syndrome may be associated with disturbed vitamin B12 transport into the CNS von Luder, A. S., Tanner, S. M., de la Chapelle, A., Walter, J. H.

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