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Human Molecular Genetics
|
July 1, 1992
Identification and characterization of a new gene in the human Xq28 region
A M van den Ouweland, P Kioschis, M Verdijk, et al.
British Journal of Haematology
|
May 1, 1994
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy: G6PD Modena
M D Cappellini, M Sampietro, D Toniolo, et al.
Reproductive Biomedicine Online
|
August 28, 2010
Normal serum concentrations of anti-Müllerian hormone in women with regular menstrual cycles
A La Marca, G Sighinolfi, S Giulini, et al.
The EMBO Journal
|
August 1, 1986
Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase
G Martini, D Toniolo, T Vulliamy, et al.
Neuromuscular Disorders : NMD
|
July 23, 1998
Immunocytochemical detection of emerin within the nuclear matrix
S Squarzoni, P Sabatelli, A Ognibene, et al.
American Journal of Human Genetics
|
January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation
E Maestrini, S Rivella, C Tribioli, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1984
Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site
P Szabo, M Purrello, M Rocchi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 23, 1996
An X chromosome-linked gene encoding a protein with characteristics of a rhoGAP predominantly expressed in hematopoietic cells
C Tribioli, S Droetto, S Bione, et al.
Human Molecular Genetics
|
July 1, 1992
An archipelago of CpG islands in Xq28: identification and fine mapping of 20 new CpG islands of the human X chromosome
E Maestrini, F Tamanini, P Kioschis, et al.
American Journal of Human Genetics
|
September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males
I Meloni, M Bruttini, I Longo, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 93) with videos related to
Sort By:
Page
of 10
Human Molecular Genetics
|
July 1, 1992
Identification and characterization of a new gene in the human Xq28 region
A M van den Ouweland, P Kioschis, M Verdijk, et al.
British Journal of Haematology
|
May 1, 1994
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy: G6PD Modena
M D Cappellini, M Sampietro, D Toniolo, et al.
Reproductive Biomedicine Online
|
August 28, 2010
Normal serum concentrations of anti-Müllerian hormone in women with regular menstrual cycles
A La Marca, G Sighinolfi, S Giulini, et al.
The EMBO Journal
|
August 1, 1986
Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenase
G Martini, D Toniolo, T Vulliamy, et al.
Neuromuscular Disorders : NMD
|
July 23, 1998
Immunocytochemical detection of emerin within the nuclear matrix
S Squarzoni, P Sabatelli, A Ognibene, et al.
American Journal of Human Genetics
|
January 1, 1992
Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation
E Maestrini, S Rivella, C Tribioli, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1984
Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site
P Szabo, M Purrello, M Rocchi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 23, 1996
An X chromosome-linked gene encoding a protein with characteristics of a rhoGAP predominantly expressed in hematopoietic cells
C Tribioli, S Droetto, S Bione, et al.
Human Molecular Genetics
|
July 1, 1992
An archipelago of CpG islands in Xq28: identification and fine mapping of 20 new CpG islands of the human X chromosome
E Maestrini, F Tamanini, P Kioschis, et al.
American Journal of Human Genetics
|
September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males
I Meloni, M Bruttini, I Longo, et al.
Page
of 10