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T Casals

Showing results (1-10 of 75) with videos related to

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Nucleic Acids Research|May 25, 1990
A polymorphic DNA probe from chromosome 7 (7q22)T Casals, V Nunes, X Estivill
Advances in Experimental Medicine and Biology|January 1, 1991
Genetic analysis of cystic fibrosisX Estivill, T Casals, V Nunes
Sangre|January 1, 1986
[Association of Hb D Punjab and beta zero thalassemia: first case in Spain]T Casals, M Baiget, J L Hernández
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.
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.
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.
Journal of Medical Genetics|May 1, 1994
A cystic fibrosis patient homozygous for the new frameshift mutation 936delTA: description and clinical dataM Chillón, T Casals, J Giménez, et al.
Human Mutation|January 1, 1994
Analysis of the CFTR gene in the Spanish population: SSCP-screening for 60 known mutations and identification of four new mutations (Q30X, A120T, 1812-1 G-->A, and 3667del4)M Chillón, T Casals, J Giménez, et al.
Human Molecular Genetics|August 1, 1993
Identification of a 31-bp insertion (3860ins31) in exon 20 of the cystic fibrosis (CFTR) geneM Chillón, T Casals, V Nunes, et al.
Pageof 8

Showing results (1-10 of 75) with videos related to

Sort By:
Pageof 8
Nucleic Acids Research|May 25, 1990
A polymorphic DNA probe from chromosome 7 (7q22)T Casals, V Nunes, X Estivill
Advances in Experimental Medicine and Biology|January 1, 1991
Genetic analysis of cystic fibrosisX Estivill, T Casals, V Nunes
Sangre|January 1, 1986
[Association of Hb D Punjab and beta zero thalassemia: first case in Spain]T Casals, M Baiget, J L Hernández
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.
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.
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.
Journal of Medical Genetics|May 1, 1994
A cystic fibrosis patient homozygous for the new frameshift mutation 936delTA: description and clinical dataM Chillón, T Casals, J Giménez, et al.
Human Mutation|January 1, 1994
Analysis of the CFTR gene in the Spanish population: SSCP-screening for 60 known mutations and identification of four new mutations (Q30X, A120T, 1812-1 G-->A, and 3667del4)M Chillón, T Casals, J Giménez, et al.
Human Molecular Genetics|August 1, 1993
Identification of a 31-bp insertion (3860ins31) in exon 20 of the cystic fibrosis (CFTR) geneM Chillón, T Casals, V Nunes, et al.
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