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Trends in Genetics : TIG
|
May 1, 1996
Rapid sequencing protocol using microconcentrators
D Petroni, C Pastore, A Lasa, et al.
Medicina Clinica
|
July 27, 2001
[Molecular analysis of the RPE65 gene in 72 Spanish families with autosomal recessive retinitis pigmentosa]
I Marcos, A Ruiz, S Borrego, et al.
Diabetes Care
|
March 31, 1999
C282Y and H63D mutations of the hemochromatosis candidate gene in type 2 diabetes
J M Fernandez-Real, J Vendrell, M Baiget, et al.
Medicina Clinica
|
March 25, 1995
[Minimal residual disease in chronic myeloid leukemia in patients with long survival after allogeneic bone marrow transplantation]
A García, J Román, S Brunet, et al.
Neurologia (Barcelona, Spain)
|
November 1, 1991
[Application of the polymerase chain reaction technique (PCR) to the molecular diagnosis of myotonic dystrophy]
A M Cobo, J M Martínez, A López de Munain, et al.
Clinical and Experimental Pharmacology & Physiology
|
August 24, 2007
Simultaneous genotyping of CYP2D6*3, *4, *5 and *6 polymorphisms in a Spanish population through multiplex long polymerase chain reaction and minisequencing multiplex single base extension analysis
A Crescenti, S Mas, P Gassó, et al.
Neurologia (Barcelona, Spain)
|
October 1, 1994
[DNA instability and neurological diseases: a new model for genetic disease]
A López de Munain, A Cobo, J F Martí Massó, et al.
Anales Espanoles De Pediatria
|
July 1, 1989
[Contribution of molecular genetics to the detection of carriers of severe genetic diseases]
M Baiget Bastus, X Estivill Palleja, P Gallano Petit, et al.
Medicina Clinica
|
December 16, 1989
[DNA polymorphisms as implant markers in allogeneic bone marrow transplantation. Preliminary evaluation]
S Brunet, T Casals, P Madoz, et al.
Neurology
|
July 14, 2004
Detection of novel mutations in the SMN Tudor domain in type I SMA patients
I Cuscó, M Jesus Barceló, E del Río, et al.
Page
of 22
Search research articles
Search
Showing results (61-70 of 217) with videos related to
Sort By:
Page
of 22
Trends in Genetics : TIG
|
May 1, 1996
Rapid sequencing protocol using microconcentrators
D Petroni, C Pastore, A Lasa, et al.
Medicina Clinica
|
July 27, 2001
[Molecular analysis of the RPE65 gene in 72 Spanish families with autosomal recessive retinitis pigmentosa]
I Marcos, A Ruiz, S Borrego, et al.
Diabetes Care
|
March 31, 1999
C282Y and H63D mutations of the hemochromatosis candidate gene in type 2 diabetes
J M Fernandez-Real, J Vendrell, M Baiget, et al.
Medicina Clinica
|
March 25, 1995
[Minimal residual disease in chronic myeloid leukemia in patients with long survival after allogeneic bone marrow transplantation]
A García, J Román, S Brunet, et al.
Neurologia (Barcelona, Spain)
|
November 1, 1991
[Application of the polymerase chain reaction technique (PCR) to the molecular diagnosis of myotonic dystrophy]
A M Cobo, J M Martínez, A López de Munain, et al.
Clinical and Experimental Pharmacology & Physiology
|
August 24, 2007
Simultaneous genotyping of CYP2D6*3, *4, *5 and *6 polymorphisms in a Spanish population through multiplex long polymerase chain reaction and minisequencing multiplex single base extension analysis
A Crescenti, S Mas, P Gassó, et al.
Neurologia (Barcelona, Spain)
|
October 1, 1994
[DNA instability and neurological diseases: a new model for genetic disease]
A López de Munain, A Cobo, J F Martí Massó, et al.
Anales Espanoles De Pediatria
|
July 1, 1989
[Contribution of molecular genetics to the detection of carriers of severe genetic diseases]
M Baiget Bastus, X Estivill Palleja, P Gallano Petit, et al.
Medicina Clinica
|
December 16, 1989
[DNA polymorphisms as implant markers in allogeneic bone marrow transplantation. Preliminary evaluation]
S Brunet, T Casals, P Madoz, et al.
Neurology
|
July 14, 2004
Detection of novel mutations in the SMN Tudor domain in type I SMA patients
I Cuscó, M Jesus Barceló, E del Río, et al.
Page
of 22