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[Neonatal screening of sickle cell disease in France]

J Bardakdjian-Michau1

  • 1Service de biochimie génétique du Pr Goossens, CHU Henri Mondor, AP-HP, 51, avenue du, Maréchal de Tassigny, 94010 Créteil France. josiane.michau@hmn.aphp.fr <josiane.michau@hmn.aphp.fr>

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|June 28, 2008
PubMed
Abstract

No abstract available in PubMed .

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Neonatal screening for sickle cell disease in France.

Journal of clinical pathology·2008

[Good practices for the study of hemoglobin].

Annales de biologie clinique·2003

[Neonatal detection of sickle cell disease].

Journal de gynecologie, obstetrique et biologie de la reproduction·2003

Abnormal hemoglobins: laboratory methods.

Hemoglobin·2001

A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry).

British journal of haematology·1999

Gamma chain heterogeneity: determination of Hb F composition by perfusion chromatography.

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