β‐globin gene cluster haplotypes in sickle cell patients from Panamá

No abstract is available for this paper.

• Publication year

  2011

• Venue

  American Journal of Human Biology

• Publication date

  2011-05-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/ajhb.21148PMID 21387457
• 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.

• β‐Globin gene cluster haplotypes and α‐thalassemia in sickle cell disease patients from Trinidad

  2008cited by this paper
• Global epidemiology of haemoglobin disorders and derived service indicators.

  2008influential reference
• Improved survival of children and adolescents with sickle cell disease.

  2008cited by this paper
• Prediction of Protein-protein Interactions on the Basis of Evolutionary Conservation of Protein Functions

  2007influential reference
• Sickle cell disease as a paradigm of immigration hematology: new challenges for hematologists in Europe.

  2007cited by this paper
• African gene flow to north Brazil as revealed by HBB*S gene haplotype analysis.

  2006cited by this paper
• Site‐specific genetic divergence in parallel hybrid zones suggests nonallopatric evolution of reproductive barriers

  2006cited by this paper
• African gene flow to north Brazil as revealed by HBB*S gene haplotype analysis

  2006cited by this paper
• Arlequin (version 3.0): An integrated software package for population genetics data analysis

  2005cited by this paper
• Beta‐globin gene cluster haplotypes as evidence of African gene flow to the northeastern coast of Venezuela

  2003cited by this paper
• Analysis of βS and βA Genes in a Mexican Population with African Roots

  2002cited by this paper
• Analysis of betaS and betaA genes in a Mexican population with African roots.

  2002cited by this paper
• Fetal Hemoglobin in Sickle Cell Anemia: Relation to Regulatory Sequences cis to the P-Globin Gene

  2002cited by this paper
• Rearrangements of the beta-globin gene cluster in apparently typical betaS haplotypes.

  2001cited by this paper
• Inherited haemoglobin disorders: an increasing global health problem.

  2001influential reference
• Sickle Cell Anemia and β-Globin Gene Cluster Haplotypes in Colombia

  2000cited by this paper
• Haplotipos de la hemoglobina S: importancia epidemiológica, antropológica y clínica

  1998cited by this paper
• [Hemoglobin S haplotypes: their epidemiologic, anthropologic and clinical importance].

  1998cited by this paper
• Methods in Molecular Medicine: Molecular Diagnosis of Genetic Diseases

  1997cited by this paper
• Fetal hemoglobin in sickle cell anemia: relation to regulatory sequences cis to the beta-globin gene. Multicenter Study of Hydroxyurea.

  1996cited by this paper
• Hemoglobinopathies : community clues to mutation detection.

  1996cited by this paper
• Further evidence on the underestimation of the prevalence of TT viral DNA in blood donors.

  1996cited by this paper
• Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia

  1995cited by this paper
• Analysis of beta-globin gene haplotypes in Asian Indians: origin and spread of beta-thalassaemia on the Indian subcontinent.

  1992cited by this paper
• Analysis of β-globin gene haplotypes in Asian Indians: origin and spread of β-thalassaemia on the Indian subcontinent

  1992cited by this paper
• Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic features.

  1991cited by this paper
• Sickle cell anemia: beta s-gene-cluster haplotypes as prognostic indicators of vital organ failure.

  1991cited by this paper
• The Senegal DNA haplotype is associated with the amelioration of anemia in African-American sickle cell anemia patients.

  1991cited by this paper
• Sickle Cell Anaemia, Genetic Variations, and the Slave Trade to the United States

  1990cited by this paper
• β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California

  1989cited by this paper
• Beta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California.

  1989cited by this paper
• Fetal hemoglobin levels and beta (s) globin haplotypes in an Indian populations with sickle cell disease.

  1987cited by this paper
• Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

  1985cited by this paper
• Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.

  1984cited by this paper
• Multiple origins of the sickle mutation: evidence from beta S globin gene cluster polymorphisms.

  1983cited by this paper
• Estimation of Small Percentages of Fœtal Hæmoglobin

  1959cited by this paper
• Abnormal human haemoglobins. III. The chemical difference between normal and sickle cell haemoglobins.

  1959cited by this paper
• Estimation of small percentages of foetal haemoglobin.

  1959cited by this paper

• PREVALENCE OF SICKLE CELL DISEASE IN PANAMA

  2026cites this paper
• Molecular characterisation of sickle cell disease and classification of major haplotypes associated with the β-globin cluster (HBB gene) by means of SNP marker sequencing in a group of samples from Bolívar, Colombia

  2024cites this paper
• Genetic Variation and Sickle Cell Disease Severity

  2023cites this paper
• To Study the β-Globin Haplotype Pattern of Descent of a Set of Linked Alleles Occurring on the Same Chromosome in the Northern Province of India

  2023influential citation
• Sickle Cell Anemia Patients Display an Intricate Cellular and Serum Biomarker Network Highlighted by TCD4+CD69+ Lymphocytes, IL-17/MIP-1β, IL-12/VEGF, and IL-10/IP-10 Axis

  2020cites this paper
• Hemoglobinopathies in Iran: An Updated Review

  2020cites this paper
• Newborn Screening for Sickle Cell Disease in the Caribbean: An Update of the Present Situation and of the Disease Prevalence

  2019cites this paper
• Haplotype Analysis of β-Thalassaemia Major and Carriers with Filipino β°-Deletion in Sabah, Malaysia

  2018cites this paper
• Presencia de haplotipos no africanos incrementa la diversidad genética en pacientes con anemia falciforme en Colombia

  2018cites this paper
• Avaliação da influência do polimorfismo IVS-14-1046 no gene ANXA2 com o desenvolvimento do acidente vascular cerebral em pacientes pediátricos com anemia falciforme

  2017cites this paper
• The effects of old and recent migration waves in the distribution of HBB*S globin gene haplotypes

  2016cites this paper
• enetic determinants and stroke in children ith sickle cell disease

  2016cites this paper
• Genetic determinants and stroke in children with sickle cell disease.

  2016cites this paper
• Sickle cell in sickle cell disease in Latin America and the United States

  2015cites this paper
• Influence of the βs haplotype and α-thalassemia on stroke development in a Brazilian population with sickle cell anaemia

  2014cites this paper
• [Beta globin haplotypes in hemoglobin S carriers in Colombia].

  2012cites this paper
• Beta-Globin Gene Cluster Haplotypes in Iranian Sickle Cell Patients: Relation to Some Hematologic

  2012cites this paper
• Haplotipos del gen de la globina beta en portadores de hemoglobina S en Colombia

  2011influential citation