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X Estivill

Showing results (31-40 of 393) with videos related to

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Gene|November 26, 1999
Cloning of the human phospholipase A2 activating protein (hPLAP) gene on the chromosome 9p21 melanoma deleted regionA Ruiz, M Nadal, S Puig, et al.
Human Genetics|September 1, 1995
Two further cases of mutation R1947X in the NF1 gene: screening for a relatively common recurrent mutationC Lázaro, H Kruyer, A Gaona, et al.
Human Genetics|December 1, 1991
Recurrence of a nonsense mutation in the NF1 gene causing classical neurofibromatosis type 1X Estivill, C Lázaro, T Casals, et al.
Medicina Clinica|November 3, 1984
[Spontaneous retroperitoneal hemorrhage and anticoagulant treatment: presentation of 4 cases and review of the literature]X Estivill, P Domingo, J Fontcuberta, et al.
Genomics|May 18, 1999
Human minibrain homologue (MNBH/DYRK1): characterization, alternative splicing, differential tissue expression, and overexpression in Down syndromeJ Guimera, C Casas, X Estivill, et al.
Journal of Medical Genetics|May 1, 1996
Renal-hepatic-pancreatic dysplasia: an autosomal recessive malformationR Torra, L Alós, J Ramos, et al.
Human Genetics|May 1, 1995
Characterisation of three microsatellite polymorphisms (D21S1262, D21S1419 and D21S1421) from band 21q22.1A Bosch, J Guimerà, D Patterson, et al.
Human Genetics|November 1, 1988
Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locusP Stanier, X Estivill, N Lench, et al.
Genomics|August 1, 1991
High conservation of sequences involved in cystic fibrosis mutations in five mammalian speciesP Gasparini, V Nunes, M Dognini, et al.
Nucleic Acids Research|April 11, 1991
MspI restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) geneA Bosch, H Kruyer, V Nunes, et al.
Pageof 40

Showing results (31-40 of 393) with videos related to

Sort By:
Pageof 40
Gene|November 26, 1999
Cloning of the human phospholipase A2 activating protein (hPLAP) gene on the chromosome 9p21 melanoma deleted regionA Ruiz, M Nadal, S Puig, et al.
Human Genetics|September 1, 1995
Two further cases of mutation R1947X in the NF1 gene: screening for a relatively common recurrent mutationC Lázaro, H Kruyer, A Gaona, et al.
Human Genetics|December 1, 1991
Recurrence of a nonsense mutation in the NF1 gene causing classical neurofibromatosis type 1X Estivill, C Lázaro, T Casals, et al.
Medicina Clinica|November 3, 1984
[Spontaneous retroperitoneal hemorrhage and anticoagulant treatment: presentation of 4 cases and review of the literature]X Estivill, P Domingo, J Fontcuberta, et al.
Genomics|May 18, 1999
Human minibrain homologue (MNBH/DYRK1): characterization, alternative splicing, differential tissue expression, and overexpression in Down syndromeJ Guimera, C Casas, X Estivill, et al.
Journal of Medical Genetics|May 1, 1996
Renal-hepatic-pancreatic dysplasia: an autosomal recessive malformationR Torra, L Alós, J Ramos, et al.
Human Genetics|May 1, 1995
Characterisation of three microsatellite polymorphisms (D21S1262, D21S1419 and D21S1421) from band 21q22.1A Bosch, J Guimerà, D Patterson, et al.
Human Genetics|November 1, 1988
Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locusP Stanier, X Estivill, N Lench, et al.
Genomics|August 1, 1991
High conservation of sequences involved in cystic fibrosis mutations in five mammalian speciesP Gasparini, V Nunes, M Dognini, et al.
Nucleic Acids Research|April 11, 1991
MspI restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) geneA Bosch, H Kruyer, V Nunes, et al.
Pageof 40