CARRIER DETECTION BY DIRECT GENE ANALYSIS IN A FAMILY WITH HAEMOPHILIA B (FACTOR IX DEFICIENCY)
- 31 January 1984
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 323 (8371) , 242-243
- https://doi.org/10.1016/s0140-6736(84)90123-5
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Detection of specific sequences among DNA fragments separated by gel electrophoresisPublished by Elsevier ,2006
- CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY)The Lancet, 1984
- Human factor IX inhibitors: immunochemical characteristics and treatment with activated concentrateClinical and Laboratory Haematology, 1983
- Gene deletions in patients with haemophilia B and anti-factor IX antibodiesNature, 1983
- Isolation of a human anti-haemophilic factor IX cDNA clone using a unique 52-base synthetic oligonucleotide probe deduced from the amino acid sequence of bovine factor IXNucleic Acids Research, 1983
- Isolation and characterization of a cDNA coding for human factor IX.Proceedings of the National Academy of Sciences, 1982
- Molecular cloning of the gene for human anti-haemophilic factor IXNature, 1982
- Genotype Assignment (Carrier Detection) in the HaemophiliasClinics in Haematology, 1979