alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.
about
Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell traitHematologic differences between African-Americans and whites: the roles of iron deficiency and alpha-thalassemia on hemoglobin levels and mean corpuscular volumeGenetic determinants of haemolysis in sickle cell anaemia.Beta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California.alpha-Thalassaemia in Sardinian infants.alpha-Thalassaemia associated with the deletion of two nucleotides at position -2 and -3 preceding the AUG codon.Prenatal diagnosis of homozygous alpha thalassaemia by direct DNA analysis of uncultured amniotic fluid cells.Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytesAge- and sex-related blood cell values in healthy black Americans.Processes of copy-number change in human DNA: the dynamics of {alpha}-globin gene deletion.Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway.Human C4 haplotypes with duplicated C4A or C4BThe William Allan Memorial Award address: Thalassemia: molecular mechanism and detection.Is the doubly deleted alpha-thalassemia gene a "fugitive" allele?The thalassemias: molecular mechanisms of human genetic disease.beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].Molecular basis for nondeletion alpha-thalassemia in American blacks. Alpha 2(116GAG----UAG).Prenatal prediction of alpha-thalassemia phenotype by endonuclease mapping of parental DNA.Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.Acquired haemoglobin H disease.Triplicated alpha-globin loci in humans.A common mutant EcoRI restriction endonuclease site in the 5' flanking portion of the human alpha-globin gene.Inherited structural polymorphism of the fourth component of human complementLinkage of alpha G-Philadelphia to alpha-thalassemia in African-Americans .Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletionsRed cell parameters in infant and children from the Arabian Peninsula.'Neutropenia' in black west IndiansGenetic analysis of C4 deficiency.Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.Comparison of haematological indices between women of four ethnic groups and the effect of oral contraceptives.Human embryonic zeta-globin chains in adult patients with alpha-thalassemias.Differences in the clinical and genotypic presentation of sickle cell disease around the world.Alpha thalassemia. A modifier of sickle cell disease.Alpha thalassemia.Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase.The interaction of coexistent alpha-thalassemia and sickle cell anemia: a model for the clinical and cellular results of diminished polymerization?The laboratory evaluation of microcytic red blood cells.Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region.Neonatal screening for sickle cell diseases in Camberwell: results and recommendations of a two year pilot study.Non-anemic homozygous beta(o) thalassemia in an African-American family: association of high fetal hemoglobin levels with beta thalassemia alleles.
P2860
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P2860
alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.
description
1979 nî lūn-bûn
@nan
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
1979年论文
@zh
1979年论文
@zh-cn
name
alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.
@en
type
label
alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.
@en
prefLabel
alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.
@en
P2093
P2860
P356
P1433
P1476
alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.
@en
P2093
Davis JR Jr
Mentzer WC
P2860
P2888
P304
P356
10.1038/280605A0
P407
P577
1979-08-01T00:00:00Z
P5875
P6179
1024058892