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X Estivill

Showing results (11-20 of 393) with videos related to

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Medicina Clinica|March 9, 1991
[DNA amplification and its application in medicine]X Estivill, V Nunes
Nucleic Acids Research|March 25, 1988
Isolation and mapping of a polymorphic DNA sequence pXH3 on chromosome X [DXS235]X Estivill, P J Scambler
Lancet (London, England)|July 18, 1987
Indirect cystic fibrosis carrier detectionM Farrall, X Estivill, R Williamson
Current Opinion in Neurology|March 31, 1999
Vestibular and hearing loss in genetic and metabolic disordersP Gasparini, X Estivill, P Fortina
Human Mutation|September 12, 2000
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexinsR Rabionet, P Gasparini, X Estivill
Medicina Clinica|February 18, 1984
[Spontaneous retroperitoneal hemorrhage and anticoagulation]X Estivill, J Fontcuberta, J Félez
Nucleic Acids Research|May 25, 1990
A polymorphic DNA probe from chromosome 7 (7q22)T Casals, V Nunes, X Estivill
Nucleic Acids Research|November 25, 1991
SSCP-polymorphism in intron 12 of the CFTR gene recognized by BcIIM Chillón, V Nunes, X Estivill
Human Mutation|January 1, 1997
Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations. The Biomed CF Mutation Analysis ConsortiumX Estivill, C Bancells, C Ramos
Human Genetics|March 1, 1994
Two CA/GT repeat polymorphisms in intron 27 of the human neurofibromatosis (NF1) geneC Lázaro, A Gaona, X Estivill
Pageof 40

Showing results (11-20 of 393) with videos related to

Sort By:
Pageof 40
Medicina Clinica|March 9, 1991
[DNA amplification and its application in medicine]X Estivill, V Nunes
Nucleic Acids Research|March 25, 1988
Isolation and mapping of a polymorphic DNA sequence pXH3 on chromosome X [DXS235]X Estivill, P J Scambler
Lancet (London, England)|July 18, 1987
Indirect cystic fibrosis carrier detectionM Farrall, X Estivill, R Williamson
Current Opinion in Neurology|March 31, 1999
Vestibular and hearing loss in genetic and metabolic disordersP Gasparini, X Estivill, P Fortina
Human Mutation|September 12, 2000
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexinsR Rabionet, P Gasparini, X Estivill
Medicina Clinica|February 18, 1984
[Spontaneous retroperitoneal hemorrhage and anticoagulation]X Estivill, J Fontcuberta, J Félez
Nucleic Acids Research|May 25, 1990
A polymorphic DNA probe from chromosome 7 (7q22)T Casals, V Nunes, X Estivill
Nucleic Acids Research|November 25, 1991
SSCP-polymorphism in intron 12 of the CFTR gene recognized by BcIIM Chillón, V Nunes, X Estivill
Human Mutation|January 1, 1997
Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations. The Biomed CF Mutation Analysis ConsortiumX Estivill, C Bancells, C Ramos
Human Genetics|March 1, 1994
Two CA/GT repeat polymorphisms in intron 27 of the human neurofibromatosis (NF1) geneC Lázaro, A Gaona, X Estivill
Pageof 40