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Human Molecular Genetics
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May 18, 2000
Barhl1, a gene belonging to a new subfamily of mammalian homeobox genes, is expressed in migrating neurons of the CNS
A Bulfone, E Menguzzato, V Broccoli, et al.
Genomics
|
August 29, 1998
Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region
E 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 16p12
F Scolari, D Puzzer, A Amoroso, et al.
FEBS Letters
|
April 16, 1998
Identification and characterization of a novel member of the dystrobrevin gene family
A 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 16q24.3
G 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 Yq
A 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 chromosome
A 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 retardation
M 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 Xp22
E 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-S232
T Meitinger, B Heye, C Petit, et al.
Page
of 20
Search research articles
Search
Showing results (121-130 of 200) with videos related to
Sort By:
Page
of 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 CNS
A Bulfone, E Menguzzato, V Broccoli, et al.
Genomics
|
August 29, 1998
Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region
E 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 16p12
F Scolari, D Puzzer, A Amoroso, et al.
FEBS Letters
|
April 16, 1998
Identification and characterization of a novel member of the dystrobrevin gene family
A 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 16q24.3
G 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 Yq
A 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 chromosome
A 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 retardation
M 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 Xp22
E 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-S232
T Meitinger, B Heye, C Petit, et al.
Page
of 20