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M Baiget

Showing results (31-40 of 217) with videos related to

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Revista Espanola De Enfermedades Digestivas|March 22, 2003
[Pharmacogenetic study of thiopurine S-methyltransferase (TPMT) and thiopurine toxicity]H Corominas, C Díaz, G Vázquez, et al.
Revista Espanola De Enfermedades Digestivas|November 10, 2006
[Phenotype of ulcerative colitis, rheumatoid arthritis, and interleukin-10 gene polymorphism]H Corominas, R Fíguls, M Riera, et al.
Clinical Genetics|September 1, 1995
A novel insertional mutation of a single base on exon 12 of the dystrophin geneA Lasa, P Gallano, J Colomer, et al.
Medicina Clinica|March 18, 1989
[Detection of carriers and prenatal diagnosis of cystic fibrosis in Spanish families using DNA markers]M Baiget, T Casals, V Nunes, et al.
Medicina Clinica|May 10, 1986
[Study of the segregation pattern of the genes responsible for hemophilia A]V Nunes, M Baiget, X Estivill, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 27, 2003
Exclusion of mosaicism in Spanish haemophilia A families with inversion of intron 22E F Tizzano, M Cornet, M Domènech, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
Modifier genes in haemophilia: their expansion in the human genomeE F Tizzano, M Cornet, M Domènech, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
Complex patterns of male germline instability and somatic mosaicism in myotonic dystrophy type 1L Martorell, D G Monckton, J Gamez, et al.
Thrombosis and Haemostasis|March 1, 1997
Inhibition of urokinase-type plasminogen activator (uPA) abrogates myogenesis in vitroP Muñoz-Cánoves, F Miralles, M Baiget, et al.
Canadian Medical Association Journal|March 24, 2010
Serum ferritin concentration and bone marrow iron storesE Gimferrer, R Ayats, N Pujol-Moix, et al.
Pageof 22

Showing results (31-40 of 217) with videos related to

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Pageof 22
Revista Espanola De Enfermedades Digestivas|March 22, 2003
[Pharmacogenetic study of thiopurine S-methyltransferase (TPMT) and thiopurine toxicity]H Corominas, C Díaz, G Vázquez, et al.
Revista Espanola De Enfermedades Digestivas|November 10, 2006
[Phenotype of ulcerative colitis, rheumatoid arthritis, and interleukin-10 gene polymorphism]H Corominas, R Fíguls, M Riera, et al.
Clinical Genetics|September 1, 1995
A novel insertional mutation of a single base on exon 12 of the dystrophin geneA Lasa, P Gallano, J Colomer, et al.
Medicina Clinica|March 18, 1989
[Detection of carriers and prenatal diagnosis of cystic fibrosis in Spanish families using DNA markers]M Baiget, T Casals, V Nunes, et al.
Medicina Clinica|May 10, 1986
[Study of the segregation pattern of the genes responsible for hemophilia A]V Nunes, M Baiget, X Estivill, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 27, 2003
Exclusion of mosaicism in Spanish haemophilia A families with inversion of intron 22E F Tizzano, M Cornet, M Domènech, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
Modifier genes in haemophilia: their expansion in the human genomeE F Tizzano, M Cornet, M Domènech, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
Complex patterns of male germline instability and somatic mosaicism in myotonic dystrophy type 1L Martorell, D G Monckton, J Gamez, et al.
Thrombosis and Haemostasis|March 1, 1997
Inhibition of urokinase-type plasminogen activator (uPA) abrogates myogenesis in vitroP Muñoz-Cánoves, F Miralles, M Baiget, et al.
Canadian Medical Association Journal|March 24, 2010
Serum ferritin concentration and bone marrow iron storesE Gimferrer, R Ayats, N Pujol-Moix, et al.
Pageof 22