M T Ross|A Ballabio|I W Craig - JoVE Visualize

Showing results (91-100 of 297) with videos related to

Pageof 30

Sort By:

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.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1996

Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp)E M Battinelli, Y Boyd, I W Craig, et al.

European Journal of Immunology|December 1, 1990

Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intactR W Hendriks, M E Kraakman, I W Craig, et al.

Human Molecular Genetics|June 1, 1992

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A geneR W Hendriks, Z Y Chen, H Hinds, et al.

Immunodeficiency|January 1, 1993

Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locusR W Hendriks, Z Y Chen, H Hinds, et al.

American Journal of Nephrology|August 26, 1999

Evidence for genetic heterogeneity in benign familial hematuriaM Piccini, G Casari, J Zhou, et al.

Pageof 30

Showing results (91-100 of 297) with videos related to

Sort By:

Pageof 30

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.

Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 1, 1996

Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp)E M Battinelli, Y Boyd, I W Craig, et al.

European Journal of Immunology|December 1, 1990

Evidence that in X-linked immunodeficiency with hyperimmunoglobulinemia M the intrinsic immunoglobulin heavy chain class switch mechanism is intactR W Hendriks, M E Kraakman, I W Craig, et al.

Human Molecular Genetics|June 1, 1992

An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5' end of the monoamine oxidase A geneR W Hendriks, Z Y Chen, H Hinds, et al.

Immunodeficiency|January 1, 1993

Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locusR W Hendriks, Z Y Chen, H Hinds, et al.

American Journal of Nephrology|August 26, 1999

Evidence for genetic heterogeneity in benign familial hematuriaM Piccini, G Casari, J Zhou, et al.

Pageof 30