Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia.
about
Mutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell diseaseAcute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.Modulation of fetal hemoglobin in sickle cell anemia.Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia.Pharmacologic induction of fetal hemoglobin synthesis: cellular and molecular mechanisms.Effect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional Studyβ-Globin chain abnormalities with coexisting α-thalassemia mutations.Sickle cell disease: from the beginning until it was recognized as a public health disease.beta S haplotypes, alpha-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I.).Molecular analysis of the beta-globin gene cluster in the Niokholo Mandenka population reveals a recent origin of the beta(S) Senegal mutation.Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia.Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction modelsModulation of the phenotypic diversity of sickle cell anemia.Homozygosity for a haplotype in the HBG2-OR51B4 region is exclusive to Arab-Indian haplotype sickle cell anemia.Comment on "Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia".Coinheritance of α-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia.Sickle cell disorder, beta-globin gene cluster haplotypes and alpha-thalassemia in neonates and adults from Guadeloupe.5' hypersensitive site-2 and fetal hemoglobin in Brazilians.β-globin gene cluster haplotypes in sickle cell patients from Panamá.Molecular characteristics of pediatric patients with sickle cell anemia and stroke.A novel approach to rapid determination of betaS-globin haplotypes: sequencing of the Agamma-IVS-II region.Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β0thalassemiaSevere Hb S-β+Thalassemia Caused by IVS-I Splice Site MutationsFemales of HbAS genotype have reduced concentration of the malaria protective deoxyhemoglobin S than males
P2860
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P2860
Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh-hant
name
Gender and haplotype effects u ...... s of adult sickle cell anemia.
@en
Gender and haplotype effects u ...... s of adult sickle cell anemia.
@nl
type
label
Gender and haplotype effects u ...... s of adult sickle cell anemia.
@en
Gender and haplotype effects u ...... s of adult sickle cell anemia.
@nl
prefLabel
Gender and haplotype effects u ...... s of adult sickle cell anemia.
@en
Gender and haplotype effects u ...... s of adult sickle cell anemia.
@nl
P2093
P356
P1476
Gender and haplotype effects u ...... s of adult sickle cell anemia.
@en
P2093
Benjamin L
Gillette P
Josifovska O
P304
P356
10.1002/AJH.2830480307
P577
1995-03-01T00:00:00Z