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M Baiget

Showing results (71-80 of 217) with videos related to

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Journal of Medical Genetics|January 1, 1994
Identification by molecular diagnosis of mosaic Turner's syndrome in an obligate carrier female for fragile X syndromeM I Tejada, E Mornet, E Tizzano, et al.
Journal of Medical Genetics|September 1, 1996
Homozygous myotonic dystrophy: clinical and molecular studies of three unrelated casesL Martorell, I Illa, J Rosell, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|November 28, 2002
Prenatal diagnosis for risk of spinal muscular atrophyI Cuscó, M J Barceló, C Soler, et al.
Blood Cells, Molecules & Diseases|March 7, 2006
Genotyping the HFE gene by melting point analysis with the LightCycler system: Pros and consV Bach, M J Barceló, A Altés, et al.
Neurology|February 15, 2001
Frequency and stability of the myotonic dystrophy type 1 premutationL Martorell, D G Monckton, A Sanchez, et al.
Sangre|January 1, 1982
[Polymorphism of human fetal hemoglobin. I. Separation of A gamma and G gamma globin chains]M Bozzo, E Del Río, T Casals, et al.
Revista Clinica Espanola|April 1, 1989
[Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics]J Benítez, E Fernández, C Ramos, et al.
Human Genetics|May 1, 1992
Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish populationA Cobo, D Grinberg, S Balcells, et al.
Haematologica|April 6, 1999
HFE mutation analysis in patients with hepatitis C virus with positive screening for iron overloadA F Remacha, M Carrasco, M P Sardá, et al.
Human Mutation|January 1, 1996
Two new variants of RAG-1 protein predicted by SSCPJ F Nomdedéu, A Lasa, R Seminago, et al.
Pageof 22

Showing results (71-80 of 217) with videos related to

Sort By:
Pageof 22
Journal of Medical Genetics|January 1, 1994
Identification by molecular diagnosis of mosaic Turner's syndrome in an obligate carrier female for fragile X syndromeM I Tejada, E Mornet, E Tizzano, et al.
Journal of Medical Genetics|September 1, 1996
Homozygous myotonic dystrophy: clinical and molecular studies of three unrelated casesL Martorell, I Illa, J Rosell, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|November 28, 2002
Prenatal diagnosis for risk of spinal muscular atrophyI Cuscó, M J Barceló, C Soler, et al.
Blood Cells, Molecules & Diseases|March 7, 2006
Genotyping the HFE gene by melting point analysis with the LightCycler system: Pros and consV Bach, M J Barceló, A Altés, et al.
Neurology|February 15, 2001
Frequency and stability of the myotonic dystrophy type 1 premutationL Martorell, D G Monckton, A Sanchez, et al.
Sangre|January 1, 1982
[Polymorphism of human fetal hemoglobin. I. Separation of A gamma and G gamma globin chains]M Bozzo, E Del Río, T Casals, et al.
Revista Clinica Espanola|April 1, 1989
[Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics]J Benítez, E Fernández, C Ramos, et al.
Human Genetics|May 1, 1992
Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish populationA Cobo, D Grinberg, S Balcells, et al.
Haematologica|April 6, 1999
HFE mutation analysis in patients with hepatitis C virus with positive screening for iron overloadA F Remacha, M Carrasco, M P Sardá, et al.
Human Mutation|January 1, 1996
Two new variants of RAG-1 protein predicted by SSCPJ F Nomdedéu, A Lasa, R Seminago, et al.
Pageof 22