Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
about
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiencySickle cell disease in Middle East Arab countriesDecline in hepatitis B infection in sickle cell anaemia and beta thalassaemia majorConsanguinity among the Saudi Arabian population.Erythrocyte reference values in Emirati people with and without α+ thalassemia.Clinical and Therapeutic Profiles of Heart Failure Patients admitted to a Tertiary Hospital, Aseer Region, Saudi Arabia.Red cell parameters in infant and children from the Arabian Peninsula.Differences in the clinical and genotypic presentation of sickle cell disease around the world.Genetic red cell disorders in Saudi Arabia: a multifaceted problem.Historical and anthropological correlates of beta S haplotypes and alpha- and beta-thalassemia alleles in the Arabian Peninsula.Sickle cell gene in the population of Saudi Arabia.
P2860
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P2860
Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
description
1982 nî lūn-bûn
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1982年の論文
@ja
1982年学术文章
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1982年学术文章
@zh
1982年学术文章
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1982年学术文章
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1982年学术文章
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1982年学术文章
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1982年學術文章
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1982年學術文章
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name
Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
@en
Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
@nl
type
label
Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
@en
Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
@nl
prefLabel
Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
@en
Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
@nl
P356
P1433
P1476
Haemoglobin disorders: a pattern for thalassaemia and haemoglobinopathies in Arabia.
@en
P2093
El-Hazmi MA
P356
10.1159/000206947
P577
1982-01-01T00:00:00Z