LIEVEN MARIE-THERESE C. VAN SPEYBROECK的合作伙伴有:Monique Maria Marcella Vermeiren、PATRICK M. VERMEIREN、JAN P.M. VAN HERCK等,他(她)在卫美恒(苏州)贸易有限公司、卫美恒(苏州)医疗器械有限公司担任高管 财产线索 线索86预估价值 商业履历 连带风险的企业0 ...
Van Broeckhoven, P. De Jonghe, A. Löfgren, A. Vandenberghe, P. Latour, et al. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study Eur J Hum Genet, 4 (1996), pp. 25-33...
Nat Genet 30:22–25 Nelis E, Erdem S, Van Den Bergh PY, Belpaire-Dethiou MC, Ceuterick C, Van Gerwen V, Cuesta A, Pedrola L, Palau F, Gabreels-Festen AA, Verellen C, Tan E, Demirci M, Van Broeckhoven C, De Jonghe P, Topaloglu H, Timmerman V (2002) Mutations in GDAP1:...
Van Broeckhoven, C.S. Karger AGCytogenetics & Cell GeneticsRaeymaekers P, DeJonghe P, Swerts L, De Winter G, Gheuens J, Martin J-J, Vandenberghe A, et al. Exclusion analysis of Charcot-Marie-Tooth neuropathy (HMSN Ia) with chro- mosome ip DNA markers. Cytogenet Cell Genet (in ...
Nelis E, Van Broeckhoven C, De Jonghe P, et al. Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative study. Eur J Hum Genet. 1996;4:25–33. ...
Ismailov SM, Fedotov VP, Dadali EL, Polyakov AV, Van Broeckhoven C, Ivanov VI, De Jonghe P, Timmerman V, Evgrafov OV (2001) A new locus for autosomal dominant Charcot–Marie–Tooth disease type 2 (CMT2F) maps to chromosome 7q11–q21. Eur J Hum Genet 9:646–650 Article CAS PubMed...
P Raeymaekers, V Timmerman, E Nelis, P De Jonghe, JE Hoogendijk, F Baas, DF Barker, JJ Martin, VM De, PA Bolhuis, C Van Broeckhoven, HMSN Collaborative Research Group Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT1a) Neuromuscul Disord, 1 (1991), ...
Nelis E, Simokovic S, Timmerman V, L o¨fgren A, Backhovens H, De Jonghe P, Martin J, Van Broeckhoven C (1997) Mutation analysis of the connexin 32 (Cx32) gene in Charcot-Marie-Tooth neuropathy type 1: identification of five new mutations. Hum Mutat 9:47-52....
Christine Van BroeckhovenElsevier BVNeurobiology of DiseaseMuller HW, Suter U, Van BC, Hanemann CO, Nelis E, Timmerman V, Sancho S, Barrio L, Bolhuis P, Dermietzel R, Frank M, Gabreels-Festen A, Gillen C, Haites N, Levi G, Mariman E, Martini R, Nave K, Rautenstrauss B, ...
Christine Van BroeckhovenElsevier Inc.Neurobiology of DiseaseMuller HW, Suter U, Van BC, Hanemann CO, Nelis E, Timmerman V, Sancho S, Barrio L, Bolhuis P, Dermietzel R, Frank M, Gabreels-Festen A, Gillen C, Haites N, Levi G, Mariman E, Martini R, Nave K, Rautenstrauss B, ...