Transient red cell aplasia in siblings: A common environmental or a common hereditary factor?

Acta Paediatrica, International Journal of Paediatrics

Volumn 87, Issue 1, 1998, Pages 43-47

  Skeppner, G ^a   Forestier, E ^b   Henter, J I ^c   Wranne, L ^a  

^a ÖREBRO MEDICAL CENTRE HOSPITAL   (Sweden)

^b UMEÅ UNIVERSITY HOSPITAL   (Sweden)

^c KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Heredity; Red cell aplasia; Siblings; Transient erythroblastopenia of childhood

Indexed keywords

ANEMIA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; ENVIRONMENTAL FACTOR; ERYTHROCYTE APLASIA; ERYTHROPOIESIS; FEMALE; GENETICS; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RETICULOCYTOSIS; RETROSPECTIVE STUDY; SIBLING;

CHILD, PRESCHOOL; DIAGNOSIS, DIFFERENTIAL; ENVIRONMENTAL EXPOSURE; ENVIRONMENTAL MONITORING; FEMALE; HLA ANTIGENS; HUMANS; INCIDENCE; INFANT; MALE; NUCLEAR FAMILY; RED-CELL APLASIA, PURE; RETROSPECTIVE STUDIES; RISK FACTORS;

EID: 0031951266     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1080/08035259850157859     Document Type: Article

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