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

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Nature Genetics|May 1, 1993

Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targetingE I Rugarli, B Lutz, S C Kuratani, et al.

Human Mutation|January 1, 1994

Deletion spanning the 5' ends of both the COL4A5 and COL4A6 genes in a patient with Alport's syndrome and leiomyomatosisA Renieri, M T Bassi, L Galli, et al.

Genes and Function|June 1, 1997

A mammalian homologue of the Drosophila retinal degeneration B gene: implications for the evolution of phototransduction mechanismsF Rubboli, A Bulfone, S Bogni, et al.

Scottish Medical Journal|August 21, 2013

Perceived tutor benefits of teaching near peers: insights from two near peer teaching programmes in South East ScotlandZ U Qureshi, K R Gibson, M T Ross, et al.

American Journal of Human Genetics|November 1, 1996

Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndromeN Mastroianni, A Bettinelli, M Bianchetti, et al.

Genomics|August 1, 1996

Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)N Mastroianni, M De Fusco, M Zollo, et al.

Genomics|November 5, 1997

Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal XpS E Fisher, A Ciccodicola, K Tanaka, et al.

Journal of Inherited Metabolic Disease|January 1, 1987

Studies on cross-reacting material to steroid sulphatase in fibroblasts from patients affected by different types of steroid sulphatase deficiencyG Parenti, A Ballabio, A T Hoogeveen, et al.

Genomics|June 1, 1997

Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulfatase gene (ARSF) from the Xp22.3 regionA A Puca, M Zollo, M Repetto, et al.

American Journal of Medical Genetics|November 1, 1991

Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiencyA Ballabio, M Zollo, R Carrozzo, et al.

Pageof 30

Showing results (121-130 of 297) with videos related to

Sort By:

Pageof 30

Nature Genetics|May 1, 1993

Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targetingE I Rugarli, B Lutz, S C Kuratani, et al.

Human Mutation|January 1, 1994

Deletion spanning the 5' ends of both the COL4A5 and COL4A6 genes in a patient with Alport's syndrome and leiomyomatosisA Renieri, M T Bassi, L Galli, et al.

Genes and Function|June 1, 1997

A mammalian homologue of the Drosophila retinal degeneration B gene: implications for the evolution of phototransduction mechanismsF Rubboli, A Bulfone, S Bogni, et al.

Scottish Medical Journal|August 21, 2013

Perceived tutor benefits of teaching near peers: insights from two near peer teaching programmes in South East ScotlandZ U Qureshi, K R Gibson, M T Ross, et al.

American Journal of Human Genetics|November 1, 1996

Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndromeN Mastroianni, A Bettinelli, M Bianchetti, et al.

Genomics|August 1, 1996

Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)N Mastroianni, M De Fusco, M Zollo, et al.

Genomics|November 5, 1997

Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal XpS E Fisher, A Ciccodicola, K Tanaka, et al.

Journal of Inherited Metabolic Disease|January 1, 1987

Studies on cross-reacting material to steroid sulphatase in fibroblasts from patients affected by different types of steroid sulphatase deficiencyG Parenti, A Ballabio, A T Hoogeveen, et al.

Genomics|June 1, 1997

Identification by shotgun sequencing, genomic organization, and functional analysis of a fourth arylsulfatase gene (ARSF) from the Xp22.3 regionA A Puca, M Zollo, M Repetto, et al.

American Journal of Medical Genetics|November 1, 1991

Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiencyA Ballabio, M Zollo, R Carrozzo, et al.

Pageof 30