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M G Mattei

Showing results (421-430 of 427) with videos related to

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Genomics|March 1, 1997
Cloning of the genes encoding two murine and human cochlear unconventional type I myosinsF Crozet, A el Amraoui, S Blanchard, et al.
Human Molecular Genetics|September 16, 1998
Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolutionI E Ehrmann, P S Ellis, S Mazeyrat, et al.
Cytogenetics and Cell Genetics|July 4, 2001
Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporterC Broccardo, J Osorio, M F Luciani, et al.
Journal of Medical Genetics|September 10, 2003
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observationsJ J Luciani, P de Mas, D Depetris, et al.
Molecular and Cellular Biology|November 30, 2000
Isolation and characterization of Suv39h2, a second histone H3 methyltransferase gene that displays testis-specific expressionD O'Carroll, H Scherthan, A H Peters, et al.
Journal of Medical Genetics|April 6, 2001
Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardationF Giraudeau, L Taine, V Biancalana, et al.
Journal of Medical Genetics|November 3, 2004
Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertilityN Machev, N Saut, G Longepied, et al.
Pageof 43

Showing results (421-430 of 427) with videos related to

Sort By:
Pageof 43
You have reached the last page of results.This site can display upto 427 results.
Genomics|March 1, 1997
Cloning of the genes encoding two murine and human cochlear unconventional type I myosinsF Crozet, A el Amraoui, S Blanchard, et al.
Human Molecular Genetics|September 16, 1998
Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolutionI E Ehrmann, P S Ellis, S Mazeyrat, et al.
Cytogenetics and Cell Genetics|July 4, 2001
Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporterC Broccardo, J Osorio, M F Luciani, et al.
Journal of Medical Genetics|September 10, 2003
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observationsJ J Luciani, P de Mas, D Depetris, et al.
Molecular and Cellular Biology|November 30, 2000
Isolation and characterization of Suv39h2, a second histone H3 methyltransferase gene that displays testis-specific expressionD O'Carroll, H Scherthan, A H Peters, et al.
Journal of Medical Genetics|April 6, 2001
Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardationF Giraudeau, L Taine, V Biancalana, et al.
Journal of Medical Genetics|November 3, 2004
Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertilityN Machev, N Saut, G Longepied, et al.
Pageof 43