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X Estivill

Showing results (1-10 of 393) with videos related to

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Nature Genetics|April 1, 1996
Complexity in a monogenic diseaseX Estivill
Medicina Clinica|September 12, 1992
[Human genetics: diagnostic and preventive impact of new genetics in medicine]X Estivill
Medicina Clinica|June 22, 1985
[Thymoma and associated immunologic changes: T lymphocytes and the regulation of hematopoiesis]X Estivill
Medicina Clinica|May 1, 1993
[The human genome project: reality and hope]X Estivill
Medicina Clinica|March 18, 1989
[Progress in the analysis of cystic fibrosis: prenatal diagnosis and carrier detection]X Estivill
Anales Espanoles De Pediatria|July 1, 1988
[Prenatal diagnosis of cystic fibrosis]X Estivill
Nucleic Acids Research|February 25, 1987
A rapid method to identify cosmids containing rare restriction sitesX Estivill, R Williamson
Journal of Medical Genetics|April 16, 1999
Allele specific oligonucleotide analysis of the common deafness mutation 35delG in the connexin 26 (GJB2) geneR Rabionet, X Estivill
Molecular and Cellular Probes|October 1, 1992
Mutation analysis of genetic diseases by asymmetric-PCR SSCP and ethidium bromide staining: application to neurofibromatosis and cystic fibrosisC Lázaro, X Estivill
Genomics|August 1, 1992
Multiplex PCR amplification of three microsatellites within the CFTR geneN Morral, X Estivill
Pageof 40

Showing results (1-10 of 393) with videos related to

Sort By:
Pageof 40
Nature Genetics|April 1, 1996
Complexity in a monogenic diseaseX Estivill
Medicina Clinica|September 12, 1992
[Human genetics: diagnostic and preventive impact of new genetics in medicine]X Estivill
Medicina Clinica|June 22, 1985
[Thymoma and associated immunologic changes: T lymphocytes and the regulation of hematopoiesis]X Estivill
Medicina Clinica|May 1, 1993
[The human genome project: reality and hope]X Estivill
Medicina Clinica|March 18, 1989
[Progress in the analysis of cystic fibrosis: prenatal diagnosis and carrier detection]X Estivill
Anales Espanoles De Pediatria|July 1, 1988
[Prenatal diagnosis of cystic fibrosis]X Estivill
Nucleic Acids Research|February 25, 1987
A rapid method to identify cosmids containing rare restriction sitesX Estivill, R Williamson
Journal of Medical Genetics|April 16, 1999
Allele specific oligonucleotide analysis of the common deafness mutation 35delG in the connexin 26 (GJB2) geneR Rabionet, X Estivill
Molecular and Cellular Probes|October 1, 1992
Mutation analysis of genetic diseases by asymmetric-PCR SSCP and ethidium bromide staining: application to neurofibromatosis and cystic fibrosisC Lázaro, X Estivill
Genomics|August 1, 1992
Multiplex PCR amplification of three microsatellites within the CFTR geneN Morral, X Estivill
Pageof 40