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A Ballabio

Showing results (121-130 of 200) with videos related to

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Human Molecular Genetics|May 18, 2000
Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNSA Bulfone, E Menguzzato, V Broccoli, et al.
Genomics|August 29, 1998
Identification and characterization of a novel serine-threonine kinase gene from the Xp22 regionE Montini, G Andolfi, A Caruso, et al.
American Journal of Human Genetics|May 20, 1999
Identification of a new locus for medullary cystic disease, on chromosome 16p12F Scolari, D Puzzer, A Amoroso, et al.
FEBS Letters|April 16, 1998
Identification and characterization of a novel member of the dystrobrevin gene familyA A Puca, V Nigro, G Piluso, et al.
American Journal of Human Genetics|June 23, 1998
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3G De Michele, M De Fusco, F Cavalcanti, et al.
Annals of Human Genetics|January 1, 1989
Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and YqA Ballabio, R Carrozzo, A Gil, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.
Genomics|April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationM Piccini, F Vitelli, M Bruttini, et al.
Genomics|May 20, 1999
Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22E Montini, G Buchner, C Spalluto, et al.
American Journal of Human Genetics|October 1, 1990
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232T Meitinger, B Heye, C Petit, et al.
Pageof 20

Showing results (121-130 of 200) with videos related to

Sort By:
Pageof 20
Human Molecular Genetics|May 18, 2000
Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNSA Bulfone, E Menguzzato, V Broccoli, et al.
Genomics|August 29, 1998
Identification and characterization of a novel serine-threonine kinase gene from the Xp22 regionE Montini, G Andolfi, A Caruso, et al.
American Journal of Human Genetics|May 20, 1999
Identification of a new locus for medullary cystic disease, on chromosome 16p12F Scolari, D Puzzer, A Amoroso, et al.
FEBS Letters|April 16, 1998
Identification and characterization of a novel member of the dystrobrevin gene familyA A Puca, V Nigro, G Piluso, et al.
American Journal of Human Genetics|June 23, 1998
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3G De Michele, M De Fusco, F Cavalcanti, et al.
Annals of Human Genetics|January 1, 1989
Molecular characterization of human X/Y translocations suggests their aetiology through aberrant exchange between homologous sequences on Xp and YqA Ballabio, R Carrozzo, A Gil, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.
Genomics|April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationM Piccini, F Vitelli, M Bruttini, et al.
Genomics|May 20, 1999
Identification of SCML2, a second human gene homologous to the Drosophila sex comb on midleg (Scm): A new gene cluster on Xp22E Montini, G Buchner, C Spalluto, et al.
American Journal of Human Genetics|October 1, 1990
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232T Meitinger, B Heye, C Petit, et al.
Pageof 20