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X Estivill

Showing results (41-50 of 393) with videos related to

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Human Genetics|November 1, 1986
Chromosome assignment and restriction fragment length polymorphism analysis of the anonymous DNA probe B79a at 7q22 (HMG8 assignment D7S13)X Estivill, J Schmidtke, R Williamson, 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.
Cytogenetics and Cell Genetics|April 25, 2000
Cloning and characterization of human FTCD on 21q22.3, a candidate gene for glutamate formiminotransferase deficiencyA Solans, X Estivill, S de la Luna
Genomics|November 5, 1997
Genomic organization, alternative splicing, and expression patterns of the DSCR1 (Down syndrome candidate region 1) geneJ J Fuentes, M A Pritchard, X Estivill
Human Genetics|December 1, 1992
A rare DNA variant in exon 15 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneM Chillón, A Palacio, V Nunes, et al.
Lancet (London, England)|August 17, 1991
Prenatal diagnosis of cystic fibrosis by multiplex PCR of mutation and microsatellite allelesX Estivill, N Morral, T Casals, et al.
Genomics|July 1, 1991
CA/GT microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingoverN Morral, V Nunes, T Casals, 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.
Contributions to Nephrology|January 1, 1997
Mutations and intragenic polymorphisms in the diagnosis of autosomal dominant polycystic kidney disease type 1C Badenas, R Torra, A Darnell, et al.
Gene|April 3, 1998
Isolation and genomic characterization of the TUPLE1/HIRA gene of the pufferfish Fugu rubripesR Llevadot, X Estivill, P Scambler, et al.
Pageof 40

Showing results (41-50 of 393) with videos related to

Sort By:
Pageof 40
Human Genetics|November 1, 1986
Chromosome assignment and restriction fragment length polymorphism analysis of the anonymous DNA probe B79a at 7q22 (HMG8 assignment D7S13)X Estivill, J Schmidtke, R Williamson, 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.
Cytogenetics and Cell Genetics|April 25, 2000
Cloning and characterization of human FTCD on 21q22.3, a candidate gene for glutamate formiminotransferase deficiencyA Solans, X Estivill, S de la Luna
Genomics|November 5, 1997
Genomic organization, alternative splicing, and expression patterns of the DSCR1 (Down syndrome candidate region 1) geneJ J Fuentes, M A Pritchard, X Estivill
Human Genetics|December 1, 1992
A rare DNA variant in exon 15 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneM Chillón, A Palacio, V Nunes, et al.
Lancet (London, England)|August 17, 1991
Prenatal diagnosis of cystic fibrosis by multiplex PCR of mutation and microsatellite allelesX Estivill, N Morral, T Casals, et al.
Genomics|July 1, 1991
CA/GT microsatellite alleles within the cystic fibrosis transmembrane conductance regulator (CFTR) gene are not generated by unequal crossingoverN Morral, V Nunes, T Casals, 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.
Contributions to Nephrology|January 1, 1997
Mutations and intragenic polymorphisms in the diagnosis of autosomal dominant polycystic kidney disease type 1C Badenas, R Torra, A Darnell, et al.
Gene|April 3, 1998
Isolation and genomic characterization of the TUPLE1/HIRA gene of the pufferfish Fugu rubripesR Llevadot, X Estivill, P Scambler, et al.
Pageof 40