Diagnosis of sickle-cell disease with a universal heteroduplex generator
- 1 December 1993
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 342 (8886-8887) , 1519-1520
- https://doi.org/10.1016/s0140-6736(05)80086-8
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Coelocentesis: a new technique for early prenatal diagnosisThe Lancet, 1993
- DNA diagnosis for the detection of sickle hemoglobinopathiesAmerican Journal of Hematology, 1993
- 1 The structure and function of normal and abnormal haemoglobinsBailliere's Clinical Haematology, 1993
- Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: a rapid and reliable diagnostic approach to beta thalassaemiaBritish Journal of Haematology, 1990
- Detection of sickle cell anaemia mutation by colour DNA amplificationThe Lancet, 1990
- Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probesNature, 1986
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985