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M Seri

Showing results (11-20 of 73) with videos related to

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Journal of Medical Genetics|March 21, 1998
Ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum: variable expression of a single syndrome?M Silengo, L Silvestro, G Capizzi, et al.
International Journal of Clinical & Laboratory Research|January 1, 1992
Molecular characterization of the P and I variants of alpha 1-antitrypsinM Seri, B Magi, C Cellesi, et al.
The Journal of Physiology|June 1, 1996
Time-dependent current decline in cyclic GMP-gated bovine channels caused by point mutations in the pore region expressed in Xenopus oocytesG Bucossi, E Eismann, F Sesti, et al.
Human Genetics|April 1, 1992
Alport syndrome caused by a 5' deletion within the COL4A5 geneA Renieri, M Seri, J C Myers, et al.
Human Molecular Genetics|May 1, 1992
De novo mutation in the COL4A5 gene converting glycine 325 to glutamic acid in Alport syndromeA Renieri, M Seri, J C Myers, et al.
Gene|March 12, 1999
Characterization of a murine gene homologous to the bovine CaCC chloride channelL Romio, L Musante, R Cinti, et al.
Neuromuscular Disorders : NMD|March 31, 2010
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN)D M Cordelli, C Garone, V Marchiani, et al.
Prenatal Diagnosis|October 30, 2013
Prenatal genetic counseling referrals for advanced maternal age: still room for improvementE Pompilii, G Astolfi, O Calabrese, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Linkage analysis in two large Italian pedigrees affected with nail patella syndromeS Melchionda, M Seri, M Carella, et al.
Atherosclerosis|March 21, 2001
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier diseaseS Bertolini, L Pisciotta, M Seri, et al.
Pageof 8

Showing results (11-20 of 73) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|March 21, 1998
Ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum: variable expression of a single syndrome?M Silengo, L Silvestro, G Capizzi, et al.
International Journal of Clinical & Laboratory Research|January 1, 1992
Molecular characterization of the P and I variants of alpha 1-antitrypsinM Seri, B Magi, C Cellesi, et al.
The Journal of Physiology|June 1, 1996
Time-dependent current decline in cyclic GMP-gated bovine channels caused by point mutations in the pore region expressed in Xenopus oocytesG Bucossi, E Eismann, F Sesti, et al.
Human Genetics|April 1, 1992
Alport syndrome caused by a 5' deletion within the COL4A5 geneA Renieri, M Seri, J C Myers, et al.
Human Molecular Genetics|May 1, 1992
De novo mutation in the COL4A5 gene converting glycine 325 to glutamic acid in Alport syndromeA Renieri, M Seri, J C Myers, et al.
Gene|March 12, 1999
Characterization of a murine gene homologous to the bovine CaCC chloride channelL Romio, L Musante, R Cinti, et al.
Neuromuscular Disorders : NMD|March 31, 2010
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN)D M Cordelli, C Garone, V Marchiani, et al.
Prenatal Diagnosis|October 30, 2013
Prenatal genetic counseling referrals for advanced maternal age: still room for improvementE Pompilii, G Astolfi, O Calabrese, et al.
European Journal of Human Genetics : EJHG|October 22, 1998
Linkage analysis in two large Italian pedigrees affected with nail patella syndromeS Melchionda, M Seri, M Carella, et al.
Atherosclerosis|March 21, 2001
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier diseaseS Bertolini, L Pisciotta, M Seri, et al.
Pageof 8