Search research articles
Contact Us
Filters
Showing results (61-70 of 97) with videos related to
Page
of 10
Sort By:
Genomics
|
March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)
I Wang, B Franco, G B Ferrero, et al.
Nature Genetics
|
November 14, 1997
X-linked situs abnormalities result from mutations in ZIC3
M Gebbia, G B Ferrero, G Pilia, et al.
Nature Genetics
|
July 1, 1993
A high resolution deletion map of human chromosome Xp22
L Schaefer, G B Ferrero, A Grillo, et al.
Clinical and Experimental Rheumatology
|
September 25, 2007
Anti-GM1 and anti-sulfatide antibodies in patients with systemic lupus erythematosus, Sjögren's syndrome, mixed cryoglobulinemia and idiopathic systemic vasculitis
M Alpa, B Ferrero, R Cavallo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 19, 2014
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability
Ilaria Gandin, Flavio Faletra, Francesca Faletra, et al.
Human Molecular Genetics
|
April 1, 1994
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels
M A van Slegtenhorst, M T Bassi, G Borsani, et al.
European Journal of Human Genetics : EJHG
|
February 17, 2018
Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply
Frédéric Brioude, Raoul Hennekam, Jet Bliek, et al.
Human Molecular Genetics
|
October 1, 1995
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3
G B Ferrero, B Franco, E J Roth, et al.
Revista Espanola De Anestesiologia Y Reanimacion
|
October 1, 1970
[Preliminary report on the use of diallyl-bis-nortoxipherine (alloferine) as a muscle relaxing agent]
R Vela Díaz, E Bordel Blanco, J Espinosa Navarro, et al.
Nature Genetics
|
November 4, 2000
Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects
R N Bamford, E Roessler, R D Burdine, et al.
Page
of 10
Search research articles
Search
Showing results (61-70 of 97) with videos related to
Sort By:
Page
of 10
Genomics
|
March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)
I Wang, B Franco, G B Ferrero, et al.
Nature Genetics
|
November 14, 1997
X-linked situs abnormalities result from mutations in ZIC3
M Gebbia, G B Ferrero, G Pilia, et al.
Nature Genetics
|
July 1, 1993
A high resolution deletion map of human chromosome Xp22
L Schaefer, G B Ferrero, A Grillo, et al.
Clinical and Experimental Rheumatology
|
September 25, 2007
Anti-GM1 and anti-sulfatide antibodies in patients with systemic lupus erythematosus, Sjögren's syndrome, mixed cryoglobulinemia and idiopathic systemic vasculitis
M Alpa, B Ferrero, R Cavallo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 19, 2014
Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability
Ilaria Gandin, Flavio Faletra, Francesca Faletra, et al.
Human Molecular Genetics
|
April 1, 1994
A gene from the Xp22.3 region shares homology with voltage-gated chloride channels
M A van Slegtenhorst, M T Bassi, G Borsani, et al.
European Journal of Human Genetics : EJHG
|
February 17, 2018
Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply
Frédéric Brioude, Raoul Hennekam, Jet Bliek, et al.
Human Molecular Genetics
|
October 1, 1995
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3
G B Ferrero, B Franco, E J Roth, et al.
Revista Espanola De Anestesiologia Y Reanimacion
|
October 1, 1970
[Preliminary report on the use of diallyl-bis-nortoxipherine (alloferine) as a muscle relaxing agent]
R Vela Díaz, E Bordel Blanco, J Espinosa Navarro, et al.
Nature Genetics
|
November 4, 2000
Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects
R N Bamford, E Roessler, R D Burdine, et al.
Page
of 10