Detection of alpha-1-antitrypsin deficiency variants by synthetic oligonucleotide hybridization
- 1 December 1987
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 170 (2-3) , 201-207
- https://doi.org/10.1016/0009-8981(87)90129-x
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Prenatal diagnosis of alpha 1 antitrypsin deficiency and estimates of fetal risk for disease.Journal of Medical Genetics, 1987
- Evaluation of "at risk" alpha 1-antitrypsin genotype SZ with synthetic oligonucleotide gene probes.Journal of Clinical Investigation, 1986
- DNA restriction fragments associated with α1-antitrypsin indicate a single origin for deficiency allele PI ZNature, 1985
- Complete sequence of the cDNA for human .alpha.1-antitrypsin and the gene for the S variantBiochemistry, 1984
- Allele-Specific Hybridization Using Oligonucleotide Probes of Very High Specific Activity: Discrimination of the Human βA- and βS-Globin GenesDNA, 1984
- Prospective study of children with α1-antitrypsin deficiency: Eight-year-old follow-upThe Journal of Pediatrics, 1984
- A New Unstable PI M Variant of a1-Antitrypsin in a Finnish IsolateHuman Heredity, 1980
- Proteases and Protease Inhibitors in Chronic Obstructive Lung DiseaseActa Medica Scandinavica, 1978
- Reliable Classification of Six Pi M Subtypes by Separator Isoelectric FocusingHuman Heredity, 1978
- α 1 -Antitrypsin Deficiency: A Variant with No Detectable α 1 -AntitrypsinScience, 1973