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A Ballabio

Showing results (91-100 of 200) with videos related to

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Genomics|July 9, 1999
Identification and characterization of AFG3L2, a novel paraplegin-related geneS Banfi, M T Bassi, G Andolfi, et al.
Oncogene|December 22, 1999
Evidence for interaction between human PRUNE and nm23-H1 NDPKinaseA Reymond, S Volorio, G Merla, et al.
Journal of Medical Genetics|June 27, 2001
Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS)H Kayserili, T C Cox, L L Cox, et al.
Genomics|July 9, 1999
Characterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3S K Prakash, I B Van den Veyver, B Franco, et al.
Genomics|September 1, 1996
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8K A Mills, K D Mathews, T Scherpbier-Heddema, et al.
Clinical Genetics|July 1, 1988
X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogeneA Ballabio, G Parenti, R Carrozzo, et al.
Genomics|July 1, 1992
Sequence analysis of a partial deletion of the human steroid sulfatase gene reveals 3 bp of homology at deletion breakpointsL F Bernatowicz, X M Li, R Carrozzo, et al.
Genomics|January 1, 1992
Isolation and characterization of a yeast artificial chromosome (YAC) contig around the human steroid sulfatase geneR Carrozzo, J Ellison, P Yen, et al.
Nature|January 3, 1991
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosomeC J Brown, A Ballabio, J L Rupert, et al.
Experimental Cell Research|December 1, 1993
Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosisT G Jensen, U B Jensen, P K Jensen, et al.
Pageof 20

Showing results (91-100 of 200) with videos related to

Sort By:
Pageof 20
Genomics|July 9, 1999
Identification and characterization of AFG3L2, a novel paraplegin-related geneS Banfi, M T Bassi, G Andolfi, et al.
Oncogene|December 22, 1999
Evidence for interaction between human PRUNE and nm23-H1 NDPKinaseA Reymond, S Volorio, G Merla, et al.
Journal of Medical Genetics|June 27, 2001
Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS)H Kayserili, T C Cox, L L Cox, et al.
Genomics|July 9, 1999
Characterization of a novel chromo domain gene in xp22.3 with homology to Drosophila msl-3S K Prakash, I B Van den Veyver, B Franco, et al.
Genomics|September 1, 1996
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8K A Mills, K D Mathews, T Scherpbier-Heddema, et al.
Clinical Genetics|July 1, 1988
X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogeneA Ballabio, G Parenti, R Carrozzo, et al.
Genomics|July 1, 1992
Sequence analysis of a partial deletion of the human steroid sulfatase gene reveals 3 bp of homology at deletion breakpointsL F Bernatowicz, X M Li, R Carrozzo, et al.
Genomics|January 1, 1992
Isolation and characterization of a yeast artificial chromosome (YAC) contig around the human steroid sulfatase geneR Carrozzo, J Ellison, P Yen, et al.
Nature|January 3, 1991
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosomeC J Brown, A Ballabio, J L Rupert, et al.
Experimental Cell Research|December 1, 1993
Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosisT G Jensen, U B Jensen, P K Jensen, et al.
Pageof 20