Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Abdul Rahman Al-Swailem"'
Autor:
R. Sulaimani, Abdul Rahman Al-Swailem, Abdul Aziz Al-Meshari, Mohsen A. F. El-Hazmi, A. M. Al-Swailem, Arjumand S. Warsy
Publikováno v:
Journal of Medical Genetics. 32:623-626
This study was conducted on 3212 Saudi families to investigate the prevalence of consanguineous marriages. The families were interviewed and the information on the relationship between the husband and wife was obtained. The overall rate of consanguin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acd3f7dbce451156847154aa01b9398f
https://doi.org/10.1136/jmg.32.8.623
https://doi.org/10.1136/jmg.32.8.623
Publikováno v:
Journal of Tropical Pediatrics. 36:223-229
Generally, individuals who are heterozygous to haemoglobin S (Hb AS) are asymptomatic and do not present any haematological or clinical manifestations. However, other associated genetic abnormalities may influence the presentation in Hb AS cases. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d4cd43e634dc94e3cc4067712a5dda2
https://doi.org/10.1093/tropej/36.5.223
https://doi.org/10.1093/tropej/36.5.223
Publikováno v:
Hemoglobin. 20(3)
A comprehensive screening program was initiated in Saudi Arabia in 1982 to determine the frequency of the sickle cell (Hb S) gene in the different regions of Saudi Arabia. Over a period of 10 years 30,055 samples were collected from 36 areas in the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffd7ec58478a88c9d143d1096e5f4cc3
https://pubmed.ncbi.nlm.nih.gov/8854129
https://pubmed.ncbi.nlm.nih.gov/8854129
Publikováno v:
Hemoglobin. 19(6)
The beta-thalassemias are a heterogeneous group with respect to molecular pathogenesis, and different populations and ethnic groups differ with respect to the predominating mutations. This variable spectrum of beta-thalassemia mutations has resulted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2fd34127ff04c2bf8a6e1ee597835b6
https://pubmed.ncbi.nlm.nih.gov/8718694
https://pubmed.ncbi.nlm.nih.gov/8718694
Publikováno v:
Human heredity. 36(1)
The frequencies of glucose-6-phosphate dehydrogenase (G-6-PD), pyruvate kinase (PK) and hexokinase (HK) deficiency were determined in different regions of Saudi Arabia. G-6-PD deficiency was found to range from 0.045 to 0.220 for the male and 0.020 t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09a834e550777e33f51c637c98d41e82
https://pubmed.ncbi.nlm.nih.gov/3949360
https://pubmed.ncbi.nlm.nih.gov/3949360
Publikováno v:
Human genetics. 74(3)
In an attempt to investigate beta-globin gene polymorphism in the Saudi population, DNA samples were analysed using restriction endonucleases, Mst II and Hpa I. Both beta A and beta S genes showed extensive polymorphism and were found to be linked to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3f8645d890ed4f02c4222d240dcec0a
https://pubmed.ncbi.nlm.nih.gov/2877940
https://pubmed.ncbi.nlm.nih.gov/2877940