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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

机译：用量化CMT1A-rep序列对Charcot-Marie-tooth 1A疾病和遗传性神经病变的分子诊断：通过量化CMT1A-REP序列：染色体变体部位重组后果的后果17P11.2-12

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A Vandenberghe; P Latour; G Chauplannaz; F Chapon; J Pouget; R Dumas; A Laguenay; E Ollagnon; M Bost; S Duthel; G Chazot; M Boucherat;
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1. 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. [J] . A Laguenay, A Vandenberghe, E Ollagnon, Clinical Chemistry: Journal of the American Association for Clinical Chemists . 1996,第7期

机译：通过定量CMT1A-REP序列的分子诊断Charcot-Marie-Tooth 1A疾病和遗传性神经病，并伴有压力性麻痹：17p11.2-12号染色体变异位点的重组结果。
2. PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies [J] . Barbara W van Paassen, Anneke J van der Kooi, Karin Y van Spaendonck-Zwarts, Orphanet journal of rare diseases . 2014,第S1期

机译：PMP22相关的神经病变：1A型Charcot-Marie-Tooth病和遗传性神经病变，伴有压力性麻痹
3. PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies [J] . Barbara W van Paassen, Anneke J van der Kooi, Karin Y van Spaendonck-Zwarts, Orphanet journal of rare diseases . 2014,第S1期

机译：PMP22相关的神经病变：1A型Charcot-Marie-Tooth病和遗传性神经病变，伴有压力性麻痹
4. 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. [O] . J. Lopes, E. LeGuern, R. Gouider, 1996

机译：在Charcot-Marie-Tooth 1A型重复序列的3.2-kb区域内的重组热点：用于遗传性神经病的分子诊断和压力性麻痹以及Charcot-Marie-Tooth 1A型分子的新工具。法国CMT合作研究小组。
5. PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies [O] . Barbara W van Paassen, Anneke J van der Kooi, Karin Y van Spaendonck-Zwarts, 2014

机译：PMP22相关的神经病：Charcot-Marie-Tooth病1A型和遗传性神经病，伴有压力性麻痹

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

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