
The HpaI restriction fragment length polymorphism linked to the beta globin gene was studied in 181 Nigerian subjects. The beta s gene was found in the 13 kilobase (kb) HpaI fragment in 98.4 percent and in the remaining 1.6 percent of the cases in the HpaI 7.6 kb fragment. The majority of beta A genes (94.2%) were found in either the 7.6 or the 7.0 kb fragment whilst the remainders (5.8%) were in the 13.0 kb fragment. The rare, but not zero, associations of beta A with the 13 kb linkage and of beta s genes with the 7.6 kb fragment would lessen the accuracy in the prenatal diagnosis of sickle cell anaemia in this population through the use of the HpaI polymorphism.
Hemoglobins, Genetic Linkage, Prenatal Diagnosis, Black People, Humans, Nigeria, Reproducibility of Results, Anemia, Sickle Cell, DNA, Deoxyribonucleases, Type II Site-Specific, Polymorphism, Restriction Fragment Length, Globins
Hemoglobins, Genetic Linkage, Prenatal Diagnosis, Black People, Humans, Nigeria, Reproducibility of Results, Anemia, Sickle Cell, DNA, Deoxyribonucleases, Type II Site-Specific, Polymorphism, Restriction Fragment Length, Globins
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 0 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
