Clinical Utility of the Addition of Molecular Genetic Testing to Newborn Screening for Hemoglobinopathies for Confirmation of Alpha-Thalassemia Trait.

Detalles Bibliográficos
Publicado en:International Journal of Neonatal Screening (IJNS) Vol. 11; no. 1; pp. 12 - 21
Autores principales: Shook, Lisa M., Haygood, Deidra, Quinn, Charles T.
Formato: research tables/charts Journal Article
Publicado: MDPI Mar2025
Acceso en línea:Ver este registro en EBSCOhost
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        atl: Clinical Utility of the Addition of Molecular Genetic Testing to Newborn Screening for Hemoglobinopathies for Confirmation of Alpha-Thalassemia Trait.
      aug:
        au:
          Shook, Lisa M.
          Haygood, Deidra
          Quinn, Charles T.
        affil: Division of Hematology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA
      sug:
        subj:
          Genetic Screening Utilization
          Neonatal Assessment
          Hemoglobinopathies
          alpha-Thalassemia Diagnosis
          Quality Improvement
          Physicians, Family Education
          Information Needs
          Human
          Ohio
          Infant, Newborn
          Multimethod Studies
          Semi-Structured Interview
          Thematic Analysis
          Convenience Sample
          Descriptive Statistics
          Sequence Analysis
          Hemoglobins Blood
          Implementation Science
          Genotype
          Professional Knowledge
          Family Education
          Blood Specimen Collection
          Venipuncture
          Social Media
          Race Factors
          Ethnic Groups
          Funding Source
          Infant, Newborn: birth-1 month
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
      ab:
    language: English
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