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E Genin

Showing results (21-30 of 67) with videos related to

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Journal of Medical Genetics|January 16, 1998
Genetic heterogeneity of Meckel syndromeJ Roume, H W Ma, M Le Merrer, et al.
Annals of Human Genetics|May 8, 2008
On the origin of the transthyretin Val30Met familial amyloid polyneuropathyC Zaros, E Genin, U Hellman, et al.
Annals of Neurology|June 21, 2001
Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31S Baulac, F Picard, A Herman, et al.
Neurology|October 27, 2004
Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single familyC Verny, N Ravisé, A-L Leutenegger, et al.
Current Medicinal Chemistry|March 28, 2013
1,2,4-Oxadiazoles identified by virtual screening and their non-covalent inhibition of the human 20S proteasomeX Maréchal, E Genin, L Qin, et al.
The Journal of Clinical Investigation|March 11, 2000
Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)A Raas-Rothschild, V Cormier-Daire, M Bao, et al.
Science (New York, N.Y.)|March 24, 2000
Rapid progression to AIDS in HIV+ individuals with a structural variant of the chemokine receptor CX3CR1S Faure, L Meyer, D Costagliola, et al.
Annals of Human Genetics|June 14, 2008
Founder effect and estimation of the age of the c.892C>T (p.Arg298Cys) mutation in LMNA associated to Charcot-Marie-Tooth subtype CMT2B1 in families from North Western AfricaT Hamadouche, Y Poitelon, E Genin, et al.
American Journal of Human Genetics|October 3, 1998
A gene for Meckel syndrome maps to chromosome 11q13J Roume, E Genin, V Cormier-Daire, et al.
The Pharmacogenomics Journal|December 11, 2013
HLA-A*31:01 and different types of carbamazepine-induced severe cutaneous adverse reactions: an international study and meta-analysisE Genin, D-P Chen, S-I Hung, et al.
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
Journal of Medical Genetics|January 16, 1998
Genetic heterogeneity of Meckel syndromeJ Roume, H W Ma, M Le Merrer, et al.
Annals of Human Genetics|May 8, 2008
On the origin of the transthyretin Val30Met familial amyloid polyneuropathyC Zaros, E Genin, U Hellman, et al.
Annals of Neurology|June 21, 2001
Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31S Baulac, F Picard, A Herman, et al.
Neurology|October 27, 2004
Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single familyC Verny, N Ravisé, A-L Leutenegger, et al.
Current Medicinal Chemistry|March 28, 2013
1,2,4-Oxadiazoles identified by virtual screening and their non-covalent inhibition of the human 20S proteasomeX Maréchal, E Genin, L Qin, et al.
The Journal of Clinical Investigation|March 11, 2000
Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)A Raas-Rothschild, V Cormier-Daire, M Bao, et al.
Science (New York, N.Y.)|March 24, 2000
Rapid progression to AIDS in HIV+ individuals with a structural variant of the chemokine receptor CX3CR1S Faure, L Meyer, D Costagliola, et al.
Annals of Human Genetics|June 14, 2008
Founder effect and estimation of the age of the c.892C>T (p.Arg298Cys) mutation in LMNA associated to Charcot-Marie-Tooth subtype CMT2B1 in families from North Western AfricaT Hamadouche, Y Poitelon, E Genin, et al.
American Journal of Human Genetics|October 3, 1998
A gene for Meckel syndrome maps to chromosome 11q13J Roume, E Genin, V Cormier-Daire, et al.
The Pharmacogenomics Journal|December 11, 2013
HLA-A*31:01 and different types of carbamazepine-induced severe cutaneous adverse reactions: an international study and meta-analysisE Genin, D-P Chen, S-I Hung, et al.
Pageof 7