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A Ballabio

Showing results (111-120 of 200) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 1, 1987
Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosisA Ballabio, G Parenti, R Carrozzo, et al.
Nature Genetics|December 1, 1992
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomesB Incerti, S Guioli, A Pragliola, et al.
American Journal of Medical Genetics|December 31, 1997
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE geneG Parenti, P Buttitta, G Meroni, et al.
Human Molecular Genetics|July 13, 1999
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during developmentG Buchner, E Montini, G Andolfi, et al.
Annales De Chirurgie|January 1, 1992
[Non-malignant esophagotracheal fistulas in adults. Experience with 35 cases]R Giudicelli, J M Sainty, A Barthélémy, et al.
Archives of Surgery (Chicago, Ill. : 1960)|February 1, 1987
Sepsis score and acute-phase protein response as predictors of outcome in septic surgical patientsL Dominioni, R Dionigi, M Zanello, et al.
Genomics|January 16, 1999
Identification and characterization of CDS2, a mammalian homolog of the Drosophila CDP-diacylglycerol synthase geneM Volta, A Bulfone, C Gattuso, et al.
American Journal of Medical Genetics|July 3, 1995
Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL geneG Parenti, M G Rizzolo, M Ghezzi, et al.
Human Molecular Genetics|July 1, 1993
The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regionsM C Wapenaar, M T Bassi, L Schaefer, et al.
Annals of Neurology|March 11, 1999
Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2R Guerrini, P Bonanni, N Nardocci, et al.
Pageof 20

Showing results (111-120 of 200) with videos related to

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Pageof 20
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1987
Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosisA Ballabio, G Parenti, R Carrozzo, et al.
Nature Genetics|December 1, 1992
Kallmann syndrome gene on the X and Y chromosomes: implications for evolutionary divergence of human sex chromosomesB Incerti, S Guioli, A Pragliola, et al.
American Journal of Medical Genetics|December 31, 1997
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE geneG Parenti, P Buttitta, G Meroni, et al.
Human Molecular Genetics|July 13, 1999
MID2, a homologue of the Opitz syndrome gene MID1: similarities in subcellular localization and differences in expression during developmentG Buchner, E Montini, G Andolfi, et al.
Annales De Chirurgie|January 1, 1992
[Non-malignant esophagotracheal fistulas in adults. Experience with 35 cases]R Giudicelli, J M Sainty, A Barthélémy, et al.
Archives of Surgery (Chicago, Ill. : 1960)|February 1, 1987
Sepsis score and acute-phase protein response as predictors of outcome in septic surgical patientsL Dominioni, R Dionigi, M Zanello, et al.
Genomics|January 16, 1999
Identification and characterization of CDS2, a mammalian homolog of the Drosophila CDP-diacylglycerol synthase geneM Volta, A Bulfone, C Gattuso, et al.
American Journal of Medical Genetics|July 3, 1995
Variable penetrance of hypogonadism in a sibship with Kallmann syndrome due to a deletion of the KAL geneG Parenti, M G Rizzolo, M Ghezzi, et al.
Human Molecular Genetics|July 1, 1993
The genes for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects (MLS): cloning and characterization of the critical regionsM C Wapenaar, M T Bassi, L Schaefer, et al.
Annals of Neurology|March 11, 1999
Autosomal recessive rolandic epilepsy with paroxysmal exercise-induced dystonia and writer's cramp: delineation of the syndrome and gene mapping to chromosome 16p12-11.2R Guerrini, P Bonanni, N Nardocci, et al.
Pageof 20