Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients.

E. LeGuern, R. Gouider, M. Gugenheim, A. Brice, N. Abbas, Y. Agid, N. Birouk, J. Lopes, S. Tardieu, P. Bouche, Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: new tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group. American Journal of Human Genetics. ,vol. 58, pp. 1223- 1230 ,(1996)

Zhang Heju, Liu Pentao, Carol A. Wise, Carlos A. Garcia, James R. Lupski, Pragna I. Patel, Stewart N. Davis, Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication. American Journal of Human Genetics. ,vol. 53, pp. 853- 863 ,(1993)

Eva Nelis, Christine Van Broeckhoven, P De Jonghe, A Löfgren, A Vandenberghe, P Latour, E Le Guern, A Brice, MARIA LUISA Mostacciuolo, F Schiavon, F Palau, S Bort, M Upadhyaya, Mariano Rocchi, Nicoletta Archidiacono, P Mandich, E Bellone, K Silander, ML Savontaus, R Navon, H Goldberg-Stern, X Estivill, V Volpini, W Friedl, K Zerres, J Tyson, S Malcolm, B Holmberg, G Holmgren, ECM Mariman, AAWM Gabreels-Festen, C Yapijakis, D Vassilopoulos, C Clark, N Haites, P Hilbert, L Van Maldergem, B Rautenstrauss, H Grehl, R Mountford, K Mann, T Bettecken, JM Burgunder, CO Hanemann, HW Müller, JM Hertz, DF Schorderet, T Küntzer, C Wolf, E Kunert, F Muntoni, P Emmerick-Bock, U Orth, A Gal, Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study European Journal of Human Genetics. ,vol. 4, pp. 25- 33 ,(1996) , 10.1159/000472166

M.A. Lehrman, D.W. Russell, J.L. Goldstein, M.S. Brown, Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia. Journal of Biological Chemistry. ,vol. 262, pp. 3354- 3361 ,(1987) , 10.1016/S0021-9258(18)61510-8

D. J. Lampe, M. E. Churchill, H. M. Robertson, A purified mariner transposase is sufficient to mediate transposition in vitro The EMBO Journal. ,vol. 15, pp. 5470- 5479 ,(1996) , 10.1002/J.1460-2075.1996.TB00930.X

R Michael Liskay, Anthea Letsou, Janet L Stachelek, Homology Requirement for Efficient Gene Conversion between Duplicated Chromosomal Sequences in Mammalian Cells Genetics. ,vol. 115, pp. 161- 167 ,(1987) , 10.1093/GENETICS/115.1.161

E Akgün, J Zahn, S Baumes, G Brown, F Liang, P J Romanienko, S Lewis, M Jasin, Palindrome resolution and recombination in the mammalian germ line. Molecular and Cellular Biology. ,vol. 17, pp. 5559- 5570 ,(1997) , 10.1128/MCB.17.9.5559

Masahiko Yamamoto, Takeshi Yasuda, Kiyoshi Hayasaka, A. Ohnishi, Hiroo Yoshikawa, Takehiko Yanagihara, Tohru Ikegami, Tatsunori Yamamoto, Hirofumi Ohashi, Tomoya Nishimura, Terunori Mitsuma, Hidenori Kiyosawa, Phillip F. Chance, G. Sobue, Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP. Human Genetics. ,vol. 99, pp. 151- 154 ,(1997) , 10.1007/S004390050330

Liu Pentao, Carol A. Wise, A. Craig Chinault, Pragna I. Patel, James R. Lupski, Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit. Nature Genetics. ,vol. 2, pp. 292- 300 ,(1992) , 10.1038/NG1292-292

P Raeymaekers, V Timmerman, E Nelis, P De Jonghe, JE Hoogenduk, F Baas, DF Barker, JJ Martin, M De Visser, PA Bolhuis, C Van Broeckhoven, HMSN Collaborative Research Group, Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a) Neuromuscular Disorders. ,vol. 1, pp. 93- 97 ,(1991) , 10.1016/0960-8966(91)90055-W