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M Seri

Showing results (41-50 of 73) with videos related to

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European Journal of Human Genetics : EJHG|January 15, 1999
Exclusion of the SCN2B gene as candidate for CMT4BA Bolino, M Seri, F Caroli, et al.
American Journal of Medical Genetics. Part A|December 31, 2013
9q31.1q31.3 deletion in two patients with similar clinical features: a newly recognized microdeletion syndrome?M Mucciolo, P Magini, A Marozza, et al.
Journal of Neurovirology|June 29, 2000
Dynamics of the reactivity to MBP in multiple sclerosisA Uccelli, G Ristori, D Giunti, et al.
Genomics|December 15, 1996
Chromosomal localization of the genes (CLNS1A and CLNS1B) coding for the swelling-dependent chloride channel IClnU O Nagl, M Erdel, A Schmarda, et al.
American Journal of Medical Genetics|May 9, 2001
Fontaine-Farriaux craniosynostosis: second report in the literatureM Priolo, T De Toni, M Baffico, et al.
Blood|October 26, 2000
Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative diseaseJ Sumegi, D Huang, A Lanyi, et al.
Human Genetics|December 22, 1999
SH2D1A mutation analysis for diagnosis of XLP in typical and atypical patientsL Yin, V Ferrand, M F Lavoué, et al.
International Journal of Molecular Medicine|December 15, 2000
Exclusion of candidate genes and chromosomal regions in familial neuroblastomaG P Tonini, C McConville, R Cusano, et al.
Human Mutation|July 5, 2001
Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11I Meloni, P Rubegni, G De Aloe, et al.
European Journal of Neurology|April 9, 2008
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genesE Panza, T Pippucci, R Cusano, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
European Journal of Human Genetics : EJHG|January 15, 1999
Exclusion of the SCN2B gene as candidate for CMT4BA Bolino, M Seri, F Caroli, et al.
American Journal of Medical Genetics. Part A|December 31, 2013
9q31.1q31.3 deletion in two patients with similar clinical features: a newly recognized microdeletion syndrome?M Mucciolo, P Magini, A Marozza, et al.
Journal of Neurovirology|June 29, 2000
Dynamics of the reactivity to MBP in multiple sclerosisA Uccelli, G Ristori, D Giunti, et al.
Genomics|December 15, 1996
Chromosomal localization of the genes (CLNS1A and CLNS1B) coding for the swelling-dependent chloride channel IClnU O Nagl, M Erdel, A Schmarda, et al.
American Journal of Medical Genetics|May 9, 2001
Fontaine-Farriaux craniosynostosis: second report in the literatureM Priolo, T De Toni, M Baffico, et al.
Blood|October 26, 2000
Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative diseaseJ Sumegi, D Huang, A Lanyi, et al.
Human Genetics|December 22, 1999
SH2D1A mutation analysis for diagnosis of XLP in typical and atypical patientsL Yin, V Ferrand, M F Lavoué, et al.
International Journal of Molecular Medicine|December 15, 2000
Exclusion of candidate genes and chromosomal regions in familial neuroblastomaG P Tonini, C McConville, R Cusano, et al.
Human Mutation|July 5, 2001
Pseudoxanthoma elasticum: Point mutations in the ABCC6 gene and a large deletion including also ABCC1 and MYH11I Meloni, P Rubegni, G De Aloe, et al.
European Journal of Neurology|April 9, 2008
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genesE Panza, T Pippucci, R Cusano, et al.
Pageof 8