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Risk of erroneous results in carrier testing for haemophilia A without prior DNA analysis in male index patients.
Fransen van de Putte, D E; Frankhuizen, W S; Vijfhuizen, L; Groenewegen, L; Tamminga, R Y J; Bouman, K; van Essen, A J; Gijsbers, A C J; Ruivenkamp, C A L; Boon, E M J.
Affiliation
  • Fransen van de Putte DE; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Frankhuizen WS; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Vijfhuizen L; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Groenewegen L; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Tamminga RYJ; University Medical Center Groningen, Beatrix Children's Hospital, University of Groningen, Groningen, The Netherlands.
  • Bouman K; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • van Essen AJ; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
  • Gijsbers ACJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Ruivenkamp CAL; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Boon EMJ; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Haemophilia ; 21(3): e237-e239, 2015 May.
Article in En | MEDLINE | ID: mdl-25655912

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Factor VIII / Diagnostic Errors / Hemophilia A / Heterozygote / Genetic Carrier Screening Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limits: Humans / Infant / Male Language: En Journal: Haemophilia Journal subject: HEMATOLOGIA Year: 2015 Document type: Article Affiliation country: Países Bajos Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Factor VIII / Diagnostic Errors / Hemophilia A / Heterozygote / Genetic Carrier Screening Type of study: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limits: Humans / Infant / Male Language: En Journal: Haemophilia Journal subject: HEMATOLOGIA Year: 2015 Document type: Article Affiliation country: Países Bajos Country of publication: Reino Unido