Initially misleading communication of carrier results after newborn genetic screening
- Author
- LA PEAN, Alison1 ; FARRELL, Michael H2
[1] Neurogenetics Branch, National Institutes of Health/National Institute of Neurological Disorders and Stroke, Bethesda, Maryland, United States
[2] Center for Patient Care and Outcomes Research, Medical College of Wisconsin, Milwaukee, Wisconsin, United States - Source
Pediatrics (Evanston). 2005, Vol 116, Num 6, pp 1499-1505, 7 p ; ref : 34 ref
- CODEN
- PEDIAU
- ISSN
- 0031-4005
- Scientific domain
- Genetics; Pediatrics
- Publisher
- American Academy of Pediatrics, Elk Grove Village, IL
- Publication country
- United States
- Document type
- Article
- Language
- English
- Author keyword
- cystic fibrosis genetic testing newborn screening patient-doctor communication sickle cell disease
- Keyword (fr)
- Anémie hématie falciforme Communication Dépistage Génétique Maladie héréditaire Mucoviscidose Nouveau né Porteur Pédiatrie Relation médecin malade Résultat Anémie hémolytique Appareil digestif pathologie Appareil respiratoire pathologie Homme Hémoglobinopathie Hémopathie Métabolisme pathologie Pancréas pathologie
- Keyword (en)
- Sickle cell anemia Communication Medical screening Genetics Genetic disease Cystic fibrosis Newborn Carrier Pediatrics Physician patient relation Result Hemolytic anemia Digestive diseases Respiratory disease Human Hemoglobinopathy Hemopathy Metabolic diseases Pancreatic disease
- Keyword (es)
- Anemia glóbulo falciforme Comunicación Descubrimiento Genética Enfermedad hereditaria Mucoviscidosis Recién nacido Portador Pediatría Relación médico paciente Resultado Anemia hemolítica Aparato digestivo patología Aparato respiratorio patología Hombre Hemoglobinopatía Hemopatía Metabolismo patología Páncreas patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19A Diseases of red blood cells / 002B19A01 Anemias. Hemoglobinopathies
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B22 Metabolic diseases / 002B22D Errors of metabolism / 002B22D05 Miscellaneous hereditary metabolic disorders
- Discipline
- Blood diseases Generalities in medical sciences Metabolic diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 17336132
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1542/peds.2005-0449 
https://dx.doi.org/10.1542/peds.2005-0449
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