Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.
about
Lower reference limits of quantitative cord glucose-6-phosphate dehydrogenase estimated from healthy term neonates according to the Clinical and Laboratory Standards Institute guidelines: a cross sectional retrospective studyAdrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cellsG6PD deficiency: a classic example of pharmacogenetics with on-going clinical implicationsG6PD deficiency at Sumba in Eastern Indonesia is prevalent, diverse and severe: implications for primaquine therapy against relapsing Vivax malariaX-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency.Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis.Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for rasburicase therapy in the context of G6PD deficiency genotype.Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effectStudies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.Hair root versus red cell individual phenotype in Sardinian heterozygotes for G6PD deficiency (Mediterranean type).Triplo-X constitution of mother explains apparent occurrence of two recombinants in sibship segregating at two closely X-linked loci (G6PD and deutan).Expression of a mutant androgen receptor in cloned fibroblasts derived from a heterozygous carrier for the syndrome of testicular feminization.Glucose 6-phosphate dehydrogenase deficiency and incidence of hematologic malignancy.A novel cytofluorometric assay for the detection and quantification of glucose-6-phosphate dehydrogenase deficiency.Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.G6PD Deficiency Does Not Enhance Susceptibility for Acquiring Helicobacter pylori Infection in Sardinian Patients.Clonal stability of blood cell lineages indicated by X-chromosomal transcriptional polymorphism.Glucose-6-phosphate dehydrogenase deficiency inhibits in vitro growth of Plasmodium falciparum.Prevalences of inherited red blood cell disorders in pregnant women of different ethnicities living along the Thailand-Myanmar border.
P2860
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P2860
Variability of red cell phenotypes between and within individuals in an unbiased sample of 77 heterozygotes for G6PD deficiency in Sardinia.
description
1976 nî lūn-bûn
@nan
1976 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1976 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1976年の論文
@ja
1976年論文
@yue
1976年論文
@zh-hant
1976年論文
@zh-hk
1976年論文
@zh-mo
1976年論文
@zh-tw
1976年论文
@wuu
name
Variability of red cell phenot ...... r G6PD deficiency in Sardinia.
@ast
Variability of red cell phenot ...... r G6PD deficiency in Sardinia.
@en
type
label
Variability of red cell phenot ...... r G6PD deficiency in Sardinia.
@ast
Variability of red cell phenot ...... r G6PD deficiency in Sardinia.
@en
prefLabel
Variability of red cell phenot ...... r G6PD deficiency in Sardinia.
@ast
Variability of red cell phenot ...... r G6PD deficiency in Sardinia.
@en
P2093
P2860
P1476
Variability of red cell phenot ...... r G6PD deficiency in Sardinia.
@en
P2093
Siniscalco M
P2860
P304
P407
P577
1976-09-01T00:00:00Z