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X Estivill

Showing results (61-70 of 393) with videos related to

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Medicina Clinica|March 9, 1985
[High-doses BCNU in diseases of the central nervous system caused by myeloma]X Estivill, J Puig, S Brunet, et al.
Biochimica Et Biophysica Acta|March 27, 2001
Characterization of human FSD1, a novel brain specific gene on chromosome 19 with paralogy to 9q31L Carim-Todd, M Escarceller, X Estivill, et al.
International Journal of Legal Medicine|January 1, 1993
Genetic variation of microsatellite markers D1S117, D6S89, D11S35, APOC2, and D21S168 in the Spanish populationJ J Fuentes, I Banchs, V Volpini, et al.
Archives of Internal Medicine|August 1, 1985
Spontaneous retroperitoneal hemorrhage during oral anticoagulant therapyX Estivill Pallejà, P Domingo, J Fontcuberta, et al.
Human Genetics|January 24, 1998
Alu-splice PCR: a simple method to isolate exon-containing fragments from cloned human genomic DNAJ J Fuentes, C Pucharcós, M Pritchard, et al.
Biochimica Et Biophysica Acta|May 9, 2001
Identification and characterization of UBXD1, a novel UBX domain-containing gene on human chromosome 19p13, and its mouse orthologL Carim-Todd, M Escarceller, X Estivill, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Identification and expression analysis of C15orf3, a novel gene on chromosome 15q21.1-->q21.2L Carim, L Sumoy, N Andreu, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?N López-Bigas, R Rabionet, M L Arbonés, et al.
Human Genetics|March 1, 1994
Three CA/GT repeat polymorphisms from loci D21S414 and D21S1234 on human chromosome 21A Bosch, S Wiemann, W Ansorge, et al.
Cytogenetics and Cell Genetics|January 21, 2000
Cloning, expression, and mapping of PDCD9, the human homolog of Gallus gallus pro-apoptotic protein p52L Carim, L Sumoy, M Nadal, et al.
Pageof 40

Showing results (61-70 of 393) with videos related to

Sort By:
Pageof 40
Medicina Clinica|March 9, 1985
[High-doses BCNU in diseases of the central nervous system caused by myeloma]X Estivill, J Puig, S Brunet, et al.
Biochimica Et Biophysica Acta|March 27, 2001
Characterization of human FSD1, a novel brain specific gene on chromosome 19 with paralogy to 9q31L Carim-Todd, M Escarceller, X Estivill, et al.
International Journal of Legal Medicine|January 1, 1993
Genetic variation of microsatellite markers D1S117, D6S89, D11S35, APOC2, and D21S168 in the Spanish populationJ J Fuentes, I Banchs, V Volpini, et al.
Archives of Internal Medicine|August 1, 1985
Spontaneous retroperitoneal hemorrhage during oral anticoagulant therapyX Estivill Pallejà, P Domingo, J Fontcuberta, et al.
Human Genetics|January 24, 1998
Alu-splice PCR: a simple method to isolate exon-containing fragments from cloned human genomic DNAJ J Fuentes, C Pucharcós, M Pritchard, et al.
Biochimica Et Biophysica Acta|May 9, 2001
Identification and characterization of UBXD1, a novel UBX domain-containing gene on human chromosome 19p13, and its mouse orthologL Carim-Todd, M Escarceller, X Estivill, et al.
Cytogenetics and Cell Genetics|June 1, 2000
Identification and expression analysis of C15orf3, a novel gene on chromosome 15q21.1-->q21.2L Carim, L Sumoy, N Andreu, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?N López-Bigas, R Rabionet, M L Arbonés, et al.
Human Genetics|March 1, 1994
Three CA/GT repeat polymorphisms from loci D21S414 and D21S1234 on human chromosome 21A Bosch, S Wiemann, W Ansorge, et al.
Cytogenetics and Cell Genetics|January 21, 2000
Cloning, expression, and mapping of PDCD9, the human homolog of Gallus gallus pro-apoptotic protein p52L Carim, L Sumoy, M Nadal, et al.
Pageof 40