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A Ballabio

Showing results (61-70 of 200) with videos related to

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Minerva Medica|July 1, 1989
[The role of esophageal manometry in the surgical treatment of epiphrenic diverticula]G Negri, P Zannini, G C Roviaro, et al.
American Journal of Human Genetics|October 3, 2000
Cloning of the gene encoding a novel integral membrane protein, mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IVM T Bassi, M Manzoni, E Monti, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
A novel X-linked member of the human zinc finger protein gene family: isolation, mapping, and expressionM Marino, N Archidiacono, A Franzé, et al.
Annals of Human Genetics|October 1, 1986
Genetics of Hunter syndrome: carrier detection, new mutations, segregation and linkage analysisD S Chase, A H Morris, A Ballabio, et al.
Human Molecular Genetics|April 1, 1996
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal regionG Meroni, B Franco, N Archidiacono, et al.
Oncogene|August 5, 2000
Mlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway?G Meroni, S Cairo, G Merla, et al.
Mechanisms of Development|October 25, 2000
MAEG, an EGF-repeat containing gene, is a new marker associated with dermatome specification and morphogenesis of its derivativesG Buchner, V Broccoli, A Bulfone, et al.
Genomics|October 1, 1993
A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short armW C Lee, G B Ferrero, A C Chinault, et al.
American Journal of Nephrology|August 26, 1999
Evidence for genetic heterogeneity in benign familial hematuriaM Piccini, G Casari, J Zhou, et al.
Genomics|April 25, 2000
Identification of a new EGF-repeat-containing gene from human Xp22: a candidate for developmental disordersG Buchner, U Orfanelli, N Quaderi, et al.
Pageof 20

Showing results (61-70 of 200) with videos related to

Sort By:
Pageof 20
Minerva Medica|July 1, 1989
[The role of esophageal manometry in the surgical treatment of epiphrenic diverticula]G Negri, P Zannini, G C Roviaro, et al.
American Journal of Human Genetics|October 3, 2000
Cloning of the gene encoding a novel integral membrane protein, mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IVM T Bassi, M Manzoni, E Monti, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1993
A novel X-linked member of the human zinc finger protein gene family: isolation, mapping, and expressionM Marino, N Archidiacono, A Franzé, et al.
Annals of Human Genetics|October 1, 1986
Genetics of Hunter syndrome: carrier detection, new mutations, segregation and linkage analysisD S Chase, A H Morris, A Ballabio, et al.
Human Molecular Genetics|April 1, 1996
Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal regionG Meroni, B Franco, N Archidiacono, et al.
Oncogene|August 5, 2000
Mlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway?G Meroni, S Cairo, G Merla, et al.
Mechanisms of Development|October 25, 2000
MAEG, an EGF-repeat containing gene, is a new marker associated with dermatome specification and morphogenesis of its derivativesG Buchner, V Broccoli, A Bulfone, et al.
Genomics|October 1, 1993
A yeast artificial chromosome contig linking the steroid sulfatase and Kallmann syndrome loci on the human X chromosome short armW C Lee, G B Ferrero, A C Chinault, et al.
American Journal of Nephrology|August 26, 1999
Evidence for genetic heterogeneity in benign familial hematuriaM Piccini, G Casari, J Zhou, et al.
Genomics|April 25, 2000
Identification of a new EGF-repeat-containing gene from human Xp22: a candidate for developmental disordersG Buchner, U Orfanelli, N Quaderi, et al.
Pageof 20