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Severe hemolytic disease of the fetus and newborn due to allo-anti-D in a patient with a partial DEL phenotype arising from the variant allele described as RHD*148+1T (RHD*01EL.31).
Turley, Elona; McGowan, Eunike C; Hyland, Catherine A; Schoeman, Elizna M; Flower, Robert L; Skoll, Amanda; Delisle, Marie-France; Nelson, Tanya; Clarke, Gwen; Au, Nicholas.
Afiliação
  • Turley E; Department of Laboratory Medicine and Pathology, University of Alberta.
  • McGowan EC; Alberta Health Services, Edmonton, Alberta, Canada.
  • Hyland CA; Research and Development, Australian Red Cross Blood Service, Kelvin Grove, Brisbane, Queensland, Australia.
  • Schoeman EM; Research and Development, Australian Red Cross Blood Service, Kelvin Grove, Brisbane, Queensland, Australia.
  • Flower RL; Research and Development, Australian Red Cross Blood Service, Kelvin Grove, Brisbane, Queensland, Australia.
  • Skoll A; Research and Development, Australian Red Cross Blood Service, Kelvin Grove, Brisbane, Queensland, Australia.
  • Delisle MF; Maternal Fetal Medicine, Department of Obstetrics and Gynecology, BC Women's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Nelson T; Maternal Fetal Medicine, Department of Obstetrics and Gynecology, BC Women's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Clarke G; Molecular Genetics Laboratory, Department of Pathology and Laboratory Medicine, BC Children's Hospital and BC Women's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
  • Au N; Department of Laboratory Medicine and Pathology, University of Alberta.
Transfusion ; 58(10): 2260-2264, 2018 10.
Article em En | MEDLINE | ID: mdl-30222865
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deleção de Sequência / Imunoglobulina rho(D) / Eritroblastose Fetal Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Deleção de Sequência / Imunoglobulina rho(D) / Eritroblastose Fetal Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2018 Tipo de documento: Article