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

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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.

Human Molecular Genetics|March 1, 1995

Cloning of a human homologue of the Xenopus laevis APX gene from the ocular albinism type 1 critical regionM V Schiaffino, M T Bassi, E I Rugarli, et al.

Human Genetics|March 1, 1986

X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosomeA Ballabio, G Parenti, P Tippett, et al.

Journal of Biotechnology|June 30, 1994

Relational genome analysis using reference libraries and hybridisation fingerprintingJ D Hoheisel, M T Ross, G Zehetner, et al.

American Journal of Human Genetics|January 23, 1999

LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosisY Segal, B Peissel, A Renieri, et al.

Human Genetics|December 1, 1987

Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndromeA Ballabio, G Sebastio, R Carrozzo, et al.

Human Mutation|January 1, 1995

Mutations in the Norrie disease geneD E Schuback, Z Y Chen, I W Craig, et al.

Genomics|July 20, 1995

High-resolution comparative mapping of the proximal region of the mouse X chromosomeH J Blair, M Ho, A P Monaco, et al.

Genomics|March 1, 1997

Localization of human liver 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB1) within a YAC contig in Xp11.21R S Batra, E Hatchwell, S Rider, et al.

Eye (London, England)|January 1, 1990

DNA analysis and recombination in X-linked retinitis pigmentosaR M Redmond, C A Graham, I W Craig, et al.

Pageof 30

Showing results (101-110 of 297) with videos related to

Sort By:

Pageof 30

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.

Human Molecular Genetics|March 1, 1995

Cloning of a human homologue of the Xenopus laevis APX gene from the ocular albinism type 1 critical regionM V Schiaffino, M T Bassi, E I Rugarli, et al.

Human Genetics|March 1, 1986

X-linked ichthyosis, due to steroid sulphatase deficiency, associated with Kallmann syndrome (hypogonadotropic hypogonadism and anosmia): linkage relationships with Xg and cloned DNA sequences from the distal short arm of the X chromosomeA Ballabio, G Parenti, P Tippett, et al.

Journal of Biotechnology|June 30, 1994

Relational genome analysis using reference libraries and hybridisation fingerprintingJ D Hoheisel, M T Ross, G Zehetner, et al.

American Journal of Human Genetics|January 23, 1999

LINE-1 elements at the sites of molecular rearrangements in Alport syndrome-diffuse leiomyomatosisY Segal, B Peissel, A Renieri, et al.

Human Genetics|December 1, 1987

Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndromeA Ballabio, G Sebastio, R Carrozzo, et al.

Human Mutation|January 1, 1995

Mutations in the Norrie disease geneD E Schuback, Z Y Chen, I W Craig, et al.

Genomics|July 20, 1995

High-resolution comparative mapping of the proximal region of the mouse X chromosomeH J Blair, M Ho, A P Monaco, et al.

Genomics|March 1, 1997

Localization of human liver 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB1) within a YAC contig in Xp11.21R S Batra, E Hatchwell, S Rider, et al.

Eye (London, England)|January 1, 1990

DNA analysis and recombination in X-linked retinitis pigmentosaR M Redmond, C A Graham, I W Craig, et al.

Pageof 30