A CLINICALLY USEFUL DNA PROBE CLOSELY LINKED TO HAEMOPHILIA A
- 7 July 1984
- journal article
- Published by Elsevier in The Lancet
- Vol. 324 (8393), 6-8
- https://doi.org/10.1016/s0140-6736(84)91995-0
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy.Archives of Disease in Childhood, 1984
- CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY)The Lancet, 1984
- Gene deletions in patients with haemophilia B and anti-factor IX antibodiesNature, 1983
- FIRST-TRIMESTER FETAL DIAGNOSIS FOR HAEMOGLOBINOPATHIES: THREE CASESThe Lancet, 1982
- Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophyNature, 1982
- ANTENATAL DIAGNOSIS OF SICKLE CELL ANAEMIA BY DIRECT ANALYSIS OF THE SICKLE MUTATIONThe Lancet, 1981
- PLASMA ASSAY OF FETAL FACTORS VIIIC AND IX FOR PRENATAL DIAGNOSIS OF HÆMOPHILIAThe Lancet, 1979
- Application of Endonuclease Mapping to the Analysis and Prenatal Diagnosis of Thalassemias Caused by Globin-Gene DeletionNew England Journal of Medicine, 1978
- Monogenic disorders.Journal of Medical Genetics, 1977
- Detection of specific sequences among DNA fragments separated by gel electrophoresisJournal of Molecular Biology, 1975