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Advances in Experimental Medicine and Biology
|
January 1, 1991
Genetic analysis of cystic fibrosis
X Estivill, T Casals, V Nunes
Cytogenetic and Genome Research
|
March 17, 2009
The emerging role of structural variations in common disorders: initial findings and discovery challenges
L Armengol, R Rabionet, X Estivill
Clinical Genetics
|
May 6, 2011
DNA methylation in neurodegenerative disorders: a missing link between genome and environment?
S Iraola-Guzmán, X Estivill, R Rabionet
Nucleic Acids Research
|
September 15, 1996
Cloning (CAG/GTC)n STSs by an Alu-(CAG/GTC)n PCR method: an approach to human chromosome 12 and spinocerebellar ataxia 2 (SCA2)
M A Pujana, V Volpini, X Estivill
Journal of Epidemiology and Community Health
|
September 19, 2000
Genes as causes: scientific fact or simplistic thinking?
F X Real, J Bertranpetit, X Estivill
Biochimica Et Biophysica Acta
|
December 19, 2000
Isolation and characterisation of a novel human gene (C9orf11) on chromosome 9p21, a region frequently deleted in human cancer
A Ruiz, M A Pujana, X Estivill
Transplantation Proceedings
|
September 29, 1999
Genetic engineering approaches for organ transplantation
J M Aran, C Fillat, X Estivill
Nucleic Acids Research
|
April 4, 1998
Large CAG/CTG repeat templates produced by PCR, usefulness for the DIRECT method of cloning genes with CAG/CTG repeat expansions
M A Pujana, V Volpini, X Estivill
Transplantation Proceedings
|
September 29, 1999
Tools of gene transfer in organ transplantation
C Fillat, J M Aran, X Estivill
Cytogenetics and Cell Genetics
|
January 1, 1997
Minibrain (MNBH) is a single copy gene mapping to human chromosome 21q22.2
J Guimera, M Pritchard, M Nadal, et al.
Page
of 40
Search research articles
Search
Showing results (21-30 of 393) with videos related to
Sort By:
Page
of 40
Advances in Experimental Medicine and Biology
|
January 1, 1991
Genetic analysis of cystic fibrosis
X Estivill, T Casals, V Nunes
Cytogenetic and Genome Research
|
March 17, 2009
The emerging role of structural variations in common disorders: initial findings and discovery challenges
L Armengol, R Rabionet, X Estivill
Clinical Genetics
|
May 6, 2011
DNA methylation in neurodegenerative disorders: a missing link between genome and environment?
S Iraola-Guzmán, X Estivill, R Rabionet
Nucleic Acids Research
|
September 15, 1996
Cloning (CAG/GTC)n STSs by an Alu-(CAG/GTC)n PCR method: an approach to human chromosome 12 and spinocerebellar ataxia 2 (SCA2)
M A Pujana, V Volpini, X Estivill
Journal of Epidemiology and Community Health
|
September 19, 2000
Genes as causes: scientific fact or simplistic thinking?
F X Real, J Bertranpetit, X Estivill
Biochimica Et Biophysica Acta
|
December 19, 2000
Isolation and characterisation of a novel human gene (C9orf11) on chromosome 9p21, a region frequently deleted in human cancer
A Ruiz, M A Pujana, X Estivill
Transplantation Proceedings
|
September 29, 1999
Genetic engineering approaches for organ transplantation
J M Aran, C Fillat, X Estivill
Nucleic Acids Research
|
April 4, 1998
Large CAG/CTG repeat templates produced by PCR, usefulness for the DIRECT method of cloning genes with CAG/CTG repeat expansions
M A Pujana, V Volpini, X Estivill
Transplantation Proceedings
|
September 29, 1999
Tools of gene transfer in organ transplantation
C Fillat, J M Aran, X Estivill
Cytogenetics and Cell Genetics
|
January 1, 1997
Minibrain (MNBH) is a single copy gene mapping to human chromosome 21q22.2
J Guimera, M Pritchard, M Nadal, et al.
Page
of 40