Alpha-thalassemia in two Mediterranean populations.

No abstract is available for this paper.

• Publication year

  1982

• Venue

  Blood

• Publication date

  1982-08-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1182/BLOOD.V60.2.509.BLOODJOURNAL602509PMID 7093530
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Hb Bart's level in cord blood and deletions of alpha-globin genes.

  1982cited by this paper
• Genetic and molecular diversity in nondeletion Hb H disease.

  1981cited by this paper
• The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletions

  1980cited by this paper
• The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions.

  1980cited by this paper
• Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype.

  1980cited by this paper
• Alpha-thalassaemia in Cyprus.

  1979cited by this paper
• alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia.

  1979cited by this paper
• Molecular basis of hemoglobin-H disease in the Mediterranean population

  1979cited by this paper
• Molecular basis of hemoglobin-H disease in the Mediterranean population.

  1979cited by this paper
• α-Globin gene organisation in blacks precludes the severe form of α-thalassaemia

  1979cited by this paper
• Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene.

  1979cited by this paper
• Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes.

  1979cited by this paper
• The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H disease.

  1979cited by this paper
• The molecular basis of α-thalassemias: Frequent occurrence of dysfunctional α loci among non-Asians with Hb H disease

  1979cited by this paper
• Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.

  1978cited by this paper
• Identification of a nondeletion defect in α-thalassemia.

  1977cited by this paper
• Identification of a nondeletion defect in alpha-thalassemia.

  1977cited by this paper
• Thalassaemia in the British

  1973cited by this paper
• The genetical interpretation of haemoglobin H disease.

  1970cited by this paper
• Mild thalassemia: the result of interactions of alpha and beta thalassemia genes.

  1970cited by this paper
• Case of Intrauterine Death Due to α-Thalassaemia

  1965cited by this paper
• CASE OF INTRAUTERINE DEATH DUE TO ALPHA-THALASSAEMIA.

  1965cited by this paper
• Hæmoglobin H Disease in Thailand: a Genetical Study

  1964cited by this paper
• Two Different Molecular Organizations Account for the Single a-Globin Gene of the a-Thalassemia-2 Genotype

  year unknowncited by this paper

• Hematological phenotypes in children according to the α-globin genotypes.

  2017cites this paper
• Biomolecular signatures of severe malarial anemia

  2016cites this paper
• Pitting of malaria parasites with formation of spherocytes and alpha thalassemia in children living in malaria holoendemic lake Victoria basin

  2011cites this paper
• Molecular Basis of α-Thalassemia in Algeria

  2008cites this paper
• Phenotypic Effect of Heterozygous a and $ # { 176 }-Thalassemia Interaction

  2005cites this paper
• Heterogeneity of the α-globin gene defects in German α-thalassemia affected families

  2004cites this paper
• α-Globin gene deletion causes α-thalassemia syndromes in two German families

  2004cites this paper
• An unexpectedly high frequency of heterozygosity for alpha-thalassemia in Ashkenazi Jews.

  2004cites this paper
• An unexpectedly high frequency of heterozygosity for α-thalassemia in Ashkenazi Jews

  2004cites this paper
• Frequency and types of deletional α+ in Northern Sardinia

  2004cites this paper
• Ultrastructural characterization of the erythroid cells in a novel case of congenital anemia.

  2003cites this paper
• ALPHA-THALASSEMIA:DELETION ANALYSIS IN IRAN

  2001cites this paper
• Phenotype–genotype correlation in Sicilian patients with Hb H

  2000cites this paper
• AKEntAnnos. The Sardinia Study of Extreme Longevity

  1999cites this paper
• Molecular study and prenatal diagnosis of alpha- and beta-thalassemias in Chinese.

  1998cites this paper
• The population genetics of the haemoglobinopathies.

  1998cites this paper
• Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem

  1998cites this paper
• Hydrops fetalis caused by alpha-thalassemia: an emerging health care problem.

  1998cites this paper
• Red blood cell phenotypes in alpha-thalassemias in the Spanish population.

  1998cites this paper
• α‐thalassemia carrier identification by DNA analysis in the screening for thalassemia

  1998cites this paper
• Presence of hemoglobinopathies in Sicily: a historic perspective.

  1997cites this paper
• Clinical experience of management of thalassemia: the Sardinian experience.

  1996cites this paper
• Control of beta-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experience.

  1996cites this paper
• 1993 William Allan award address.

  1994cites this paper
• The population genetics of the haemoglobinopathies.

  1993cites this paper
• Alpha thalassaemia in Saudis.

  1992cites this paper
• Beta-thalassaemia: molecular pathogenesis and clinical variability.

  1992cites this paper
• β-thalassaemia: Molecular pathogenesis and clinical variability

  1992cites this paper
• Hemoglobinopathies in Sardinia.

  1992cites this paper
• β-Thalassämie: Molekulare Pathogenese und klinische Variabilität

  1991cites this paper
• Percentile curves for red cell indices of beta zero-thalassaemia heterozygotes in infancy and childhood.

  1991cites this paper
• [Beta thalassemia: molecular pathogenesis and clinical variability].

  1991cites this paper
• Percentile curves for red cell indices of 413-1413-1413-1heterozygotes in infancy and childhood

  1991cites this paper
• Population-based genetic screening.

  1991cites this paper
• Clinical Research Update: Thalassemias in Sardinia Molecular Pathology, Phenotype‐Genotype Correlation, and Prevention

  1991cites this paper
• Iron stores and iron deficiency anemia in children heterozygous for beta-thalassemia.

  1990cites this paper
• Fetal hydrops in Sardinia: implications for genetic counselling

  1990cites this paper
• Frequency and molecular types of deletional α-thalassemia in Egypt

  1989cites this paper
• Frequency and molecular types of deletional alpha-thalassemia in Egypt.

  1989cites this paper
• Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysis.

  1988cites this paper
• Hb G-Philadelphia, or [alpha 68(E17)Asn----Lys], in north Sardinia: detection by isoelectric focusing and identification by HPLC of tryptic peptides.

  1988cites this paper
• Homozygous βd`-39 Mutation with Thalassemia Intermedia in Northern Sardinia: Clinical, Hematological and Molecular Analysis

  1988cites this paper
• Different severity of homozygous β-thalassemia among siblings

  1987cites this paper
• Alpha-thalassemia haplotypes in the Algerian population.

  1987cites this paper
• An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype.

  1987cites this paper
• Different severity of homozygous beta-thalassemia among siblings.

  1987cites this paper
• α-Thalassemia haplotypes in the Algerian population

  1987cites this paper
• First‐trimester prenatal diagnosis of severe alpha‐thalassemia

  1986cites this paper
• The level of Hb F-Sardinia (alpha 2A gamma 2(75)Ile----Thr) in the fetal hemoglobin of Sardinian beta-thalassemic homozygotes determined by isoelectric focusing.

  1986cites this paper
• Alpha thalassaemia in an Italian population

  1986cites this paper
• The gamma globin chain heterogeneity of the Sardinian newborn baby.

  1986cites this paper
• The level of Hb F‐sardinia (α2A γ2 75IIe→Thr) in the fetal hemoglobin of sardinian β‐thalassemic homozygotes determined by isoelectric focusing

  1986cites this paper
• Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypes.

  1986influential citation
• Heterogeneity of the alpha-globin gene defects in German alpha-thalassemia affected families.

  1985cites this paper
• Frequency and types of deletional alpha+-thalassemia in northern Sardinia.

  1985cites this paper
• Concomitant inheritance of alpha-thalassemia in beta 0- thalassemia/Hb E disease.

  1985cites this paper
• Concomitant inheritance of α‐thalassemia in β°‐thalassemia/hb e disease

  1985cites this paper
• Extremely high frequencies of alpha-globin gene deletion in Madang and on Kar Kar Island, Papua New Guinea.

  1985cites this paper
• Hematological phenotype of carriers of deletion alpha-thalassemia according to the alpha-globin genotype.

  1985cites this paper
• Alpha-globin gene deletion causes alpha-thalassemia syndromes in two German families.

  1984cites this paper
• Human embryonic zeta-globin chains in adult patients with alpha-thalassemias.

  1984cites this paper
• Advances in thalassemia research.

  1984cites this paper
• Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J Sardegna.

  1984cites this paper
• Somatic-Cell Mutation Monitoring System Based on Human Hemoglobin Mutants

  1984cites this paper
• Alpha thalassaemia in Sardinian newborns

  1984cites this paper
• Hemoglobin Constitution of Double Heterozygotes for α or β-Thalassemia and HB J Sardegna

  1984cites this paper
• Developmental pattern of beta-chain production at midtrimester pregnancy in Sardinian beta o-thalassemia heterozygotes.

  1984cites this paper
• THALASSEMIA

  1984cites this paper
• Phenotypic effect of heterozygous alpha and beta 0-thalassemia interaction.

  1983cites this paper
• Molecular mechanism accounting for milder types of thalassemia major.

  1983cites this paper