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V Timmerman

Showing results (11-20 of 105) with videos related to

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Neurology|June 1, 1997
Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17qM Wehnert, V Timmerman, P Spoelders, et al.
Neurology|January 15, 2000
Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I lociM Auer-Grumbach, K Wagner, V Timmerman, et al.
Journal of the Peripheral Nervous System : JPNS|January 1, 1997
Charcot-Marie-Tooth disease and related peripheral neuropathiesP De Jonghe, V Timmerman, E Nelis, et al.
American Journal of Human Genetics|September 5, 2001
Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1K Verhoeven, M Villanova, A Rossi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 geneM Bähr, F Andres, V Timmerman, et al.
Neurology|November 30, 2000
Phenotype-genotype correlations in a CMT2B family with refined 3q13-q22 locusM Auer-Grumbach, P De Jonghe, K Wagner, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Molecular diagnostic testing in Charcot-Marie-Tooth disease and related disorders. Approaches and resultsP De Jonghe, E Nelis, V Timmerman, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Construction of a PAC contig within the distal hereditary motor neuropathy type II candidate region at 12q24J Irobi, V Timmerman, P De Jonghe, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular GeneticsV Timmerman, J Beuten, J Irobi, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Distal hereditary motor neuropathy type II (distal HMN type II): phenotype and molecular geneticsV Timmerman, J Beuten, J Irobi, et al.
Pageof 11

Showing results (11-20 of 105) with videos related to

Sort By:
Pageof 11
Neurology|June 1, 1997
Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17qM Wehnert, V Timmerman, P Spoelders, et al.
Neurology|January 15, 2000
Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I lociM Auer-Grumbach, K Wagner, V Timmerman, et al.
Journal of the Peripheral Nervous System : JPNS|January 1, 1997
Charcot-Marie-Tooth disease and related peripheral neuropathiesP De Jonghe, V Timmerman, E Nelis, et al.
American Journal of Human Genetics|September 5, 2001
Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1K Verhoeven, M Villanova, A Rossi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 geneM Bähr, F Andres, V Timmerman, et al.
Neurology|November 30, 2000
Phenotype-genotype correlations in a CMT2B family with refined 3q13-q22 locusM Auer-Grumbach, P De Jonghe, K Wagner, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Molecular diagnostic testing in Charcot-Marie-Tooth disease and related disorders. Approaches and resultsP De Jonghe, E Nelis, V Timmerman, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Construction of a PAC contig within the distal hereditary motor neuropathy type II candidate region at 12q24J Irobi, V Timmerman, P De Jonghe, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Distal Hereditary Motor Neuropathy Type II (Distal HMN Type II): Phenotype and Molecular GeneticsV Timmerman, J Beuten, J Irobi, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Distal hereditary motor neuropathy type II (distal HMN type II): phenotype and molecular geneticsV Timmerman, J Beuten, J Irobi, et al.
Pageof 11