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Molecular diagnosis of Charcot-Marie-Tooth 1A disease and hereditary neuropathy with liability to pressure palsies by quantifying CMT1A-REP sequences: consequences of recombinations at variant sites on chromosomes 17p11.2-12.
Vandenberghe A, Latour P, Chauplannaz G, Chapon F, Pouget J, Dumas R, Laguenay A, Ollagnon E, Bost M, Duthel S, Chazot G, Boucherat M. Vandenberghe A, et al. Among authors: bost m. Clin Chem. 1996 Jul;42(7):1021-5. Clin Chem. 1996. PMID: 8674184
A RsaI RFLP at the human myelin protein zero (MPZ) locus.
Latour P, Bonnebouche C, Bost M, Diraison P, Chapon F, Boucherat M, Vandenberghe A. Latour P, et al. Among authors: bost m. Clin Genet. 1994 Oct;46(4):327-8. doi: 10.1111/j.1399-0004.1994.tb04172.x. Clin Genet. 1994. PMID: 7530611 No abstract available.
[Steinert disease].
Bouhour F, Bost M, Vial C. Bouhour F, et al. Among authors: bost m. Presse Med. 2007 Jun;36(6 Pt 2):965-71. doi: 10.1016/j.lpm.2007.01.002. Epub 2007 Feb 7. Presse Med. 2007. PMID: 17289339 Review. French.
285 results