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Vol. 27. Issue 3.
Pages 147-152 (April 1991)
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Vol. 27. Issue 3.
Pages 147-152 (April 1991)
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Aportaciones de la genética molecular al estudio de la patología respiratoria
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M. Baiget, E. Tizzano
Unitat de Genética Molecular. Hospital de la Santa Creu i Sant Pau. Barcelona
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Bibliografía
[1.]
E. Southern.
Detection of specifíc sequences among DNA frag-ments separated by gel electrophoresis.
J Mol Biol, 98 (1975), pp. 503-508
[2.]
R.K. Saiki, D.H. Gelfand, S. Stoffel, et al.
Primer-directe enzymatic amplification of DNA with the thermostable DNA polymerase.
Science, 239 (1988), pp. 487-491
[3.]
R.G. Crystal.
The αl-antitrypsin gene and its deficiency states.
TIG December, 5 (1989), pp. 411-417
[4.]
J.R. Riordan, J.M. Rommens, B. Kerem, et al.
Identification of the cystic fíbrosis gene: cloning and characterization of complementary DNA.
Science, 245 (1989), pp. 1.066-1.072
[5.]
B. Kerem, J.M. Romens, J.A. Buchanan, et al.
Identification of the cystic fibrosis gene: genetic analysis.
Science, 245 (1989), pp. 1.073-1.080
[6.]
C.R. Newton, A. Graham, L.E. Heptinstall, et al.
Analysis of any point mutation in DNA.
The amplification refractory mutation system. Nucleic Acids Res, 17 (1989), pp. 2.503-2.516
[7.]
R.A. Gatti, I. Berket, E. Boder, et al.
Localization of an ataxiatelangiectasia gene to ehromosome 1 lq22-23.
Nature, 336 (1988), pp. 577-580
[8.]
S.P. Kwan, J. Terwilliger, R. Parmley, et al.
Identification of a closely linked DNA marker to further refine the X-linked agammaglobulinemia locus.
Genomics, 6 (1990), pp. 238-242
[9.]
G. Saint Basile, B. Arveiler, I. Oberlé, et al.
Close linkage of the locus for X chromosome-linked severe combined inmunodeficiency to polymorphic DNA markers in Xqll-ql3.
Proc Natl Acad Sci USA, 84 (1987), pp. 7576-7579
[10.]
G. Saint Basile, B. Arveiler, N.J. Fraser, et al.
Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndrome.
Lancet, 11 (1989), pp. 1.319-1.321
[11.]
B. Royer-Pokora, L.M. Kunkel, A.P. Monaco, et al.
Cloning the gene for an inherited human disorder-chronic granulomatous disease-on the basis of its chromosomal location.
Nature, 322 (1986), pp. 32-38
[12.]
D. Goundis, S.M. Holt, Y. Boyd, K.B.M. Reid.
Localization of the properdin structural locus to Xpl 1.23-Xp21.1.
Genomics, 5 (1989), pp. 56-60
[13.]
S.C. Jhanwar, T.M. Berkvens, C. Breukel, H. van Ormondt, A.J. van der Eb, P. Meera Khan.
Localization of human adenosine deami-nase gene sequences to the ql2-ql 3.11 region of chromosome 20 by in situ hybridization.
Cytogenet Cell Genet, 50 (1989), pp. 168-171
[14.]
J.C. Skare, A. Milunsky, K.S. Byron, J. Sullivan.
Mapping the X-linked lymphoproliferative syndrome.
Proc Nati Acad Sci USA, 84 (1987), pp. 2.015-2.018
[15.]
E.J.B.M. Mensink, A. Thompson, L.A. Sandkuyl, et al.
X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment lenght polymorphism locus.
Hum Genet, 76 (1987), pp. 96-99
[16.]
T.D. Palmer, R.A. Hock, W.R.A. Osborne, A.D. Miller.
Efficient retrovirus-mediated transfer and expressions of a human adenosine deaminase gene in diploid skin fibroblasts from a adenosine deaminase-deficient human.
Proc Natl Acad Sci. USA, (1987-84), pp. 1.055-1.059
[17.]
D.T. Kinsburg.
DNA probes in the diagnosis of genetic and infectious diseases.
TIBTECH, 5 (1987), pp. 107-111
[18.]
D. Hala, F. Kuze, Y. Mochizuki, et al.
Evaluation of DNA probe test for rapid diagnosis of Mycoplasma pneumoniase infections.
J of Pediatrics, 116 (1990), pp. 273-276
[19.]
A. Brisson-Noel, B. Gicquel, D. Lecossier, V. Levy-Frebault, X. Nassif, A.J. Hance.
Rapid diagnosis of tuberculosis by amplification of mycobacterial DNA in clinical samples.
Lancet, 11 (1989), pp. 1.069-1. 071
[20.]
J. Minna.
Genetic events in the pathogenesis of lung cancer.
Chest, 96 (1989), pp. 175-235
[21.]
D. Compton, M. Weil, L. Bonetta, et al.
Definition of the limits of the Wilms tumor locus on human ehromosome 1 lpl3.
Genomics, 6 (1990), pp. 309-315
[22.]
T.P. Dryja, J.M. Rapaport, J. Joyce, R.A. Petersen.
Molecular detection of deletion involving band ql4 of chromosome 13 in retinoblastomas.
Proc Natl Acad Sci USA, 83 (1986), pp. 7.391-7.394
Copyright © 1991. Sociedad Española de Neumología y Cirugía Torácica
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