SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1756-0500
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon ; volume:10 ; number:1 ; day:12 ; month:5 ; year:2017 ; pages:1-5 ; date:12.2017
BMC Research Notes / Biomed Central; 10, Heft 1 (12.5.2017), 1-5, 12.2017
- Keyword
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Erbkrankheit
Erbschaden
- Creator
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Pule, Gift Dineo
- Contributor
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Bitoungui, Valentina Josiane Ngo
Chemegni, Bernard Chetcha
Kengne, André Pascal
Wonkam, Ambroise
SpringerLink (Online service)
- DOI
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10.1186/s13104-017-2502-3
- URN
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urn:nbn:de:1111-201705222651
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:38 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Pule, Gift Dineo
- Bitoungui, Valentina Josiane Ngo
- Chemegni, Bernard Chetcha
- Kengne, André Pascal
- Wonkam, Ambroise
- SpringerLink (Online service)
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Fetal hemoglobin level and nutritional status in patients with sickle cell disease
Correlates of Pulmonary Function in Children with Sickle Cell Disease and Elevated Fetal Hemoglobin
High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania
Malaria in patients with sickle cell anaemia: burden, risk factors and outcome at the Laquintinie hospital, Cameroon
Immunoglobulin G responses against falciparum malaria specific antigens are higher in children with homozygous sickle cell trait than those with normal hemoglobin
The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease
Gum Arabic as fetal hemoglobin inducing agent in sickle cell anemia; in vivo study
Understanding the aggregation of sickle hemoglobin (HbS) and identification of HbS aggregation inhibitors
Burden and spectrum of bacterial infections among sickle cell disease children living in Cameroon
Hemoglobin determination with paired emitter detector diode
Central sensitization associated with low fetal hemoglobin levels in adults with sickle cell anemia
Fetal hemoglobin level and nutritional status in patients with sickle cell disease
Correlates of Pulmonary Function in Children with Sickle Cell Disease and Elevated Fetal Hemoglobin
High fetal hemoglobin level is associated with increased risk of cerebral vasculopathy in children with sickle cell disease in Mayotte
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania
Malaria in patients with sickle cell anaemia: burden, risk factors and outcome at the Laquintinie hospital, Cameroon
Immunoglobulin G responses against falciparum malaria specific antigens are higher in children with homozygous sickle cell trait than those with normal hemoglobin
The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease
Gum Arabic as fetal hemoglobin inducing agent in sickle cell anemia; in vivo study
Understanding the aggregation of sickle hemoglobin (HbS) and identification of HbS aggregation inhibitors
Burden and spectrum of bacterial infections among sickle cell disease children living in Cameroon