- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2431
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Erratum to: Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant ; volume:16 ; number:1 ; day:9 ; month:12 ; year:2016 ; pages:1 ; date:12.2016
BMC pediatrics ; 16, Heft 1 (9.12.2016), 1, 12.2016
- Creator
-
Moiz, Bushra
- Contributor
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Nasir, Amna
Khan, Sarosh Ahmed
Kherani, Saleema Amin
Qadir, Maqbool
SpringerLink (Online service)
- DOI
-
10.1186/s12887-016-0752-1
- URN
-
urn:nbn:de:1111-201701065913
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:48 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Moiz, Bushra
- Nasir, Amna
- Khan, Sarosh Ahmed
- Kherani, Saleema Amin
- Qadir, Maqbool
- SpringerLink (Online service)
Other Objects (12)
Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
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Effect of neonatal reticulocytosis on glucose 6-phosphate dehydrogenase (G6PD) activity and G6PD deficiency detection: a cross-sectional study
Hemolytic crisis in a G6PD-deficient infant after ingestion of pumpkin
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
A novel G6PD deleterious variant identified in three families with severe glucose-6-phosphate dehydrogenase deficiency
Novel TRPV6 variant linked with transient neonatal hyperparathyroidism
Assessment of CareStart G6PD rapid diagnostic test and CareStart G6PD biosensor in Mauritania
Charakterisierung von G6PD-Mutanten [GPD-Mutanten]
Spectrophotometry assays to determine G6PD activity from Trinity Biotech and Pointe Scientific G6PD show good correlation
G6PD testing in support of treatment and elimination of malaria: recommendations for evaluation of G6PD tests
Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population
Effect of neonatal reticulocytosis on glucose 6-phosphate dehydrogenase (G6PD) activity and G6PD deficiency detection: a cross-sectional study
Hemolytic crisis in a G6PD-deficient infant after ingestion of pumpkin
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
A novel G6PD deleterious variant identified in three families with severe glucose-6-phosphate dehydrogenase deficiency
Novel TRPV6 variant linked with transient neonatal hyperparathyroidism
Assessment of CareStart G6PD rapid diagnostic test and CareStart G6PD biosensor in Mauritania
Charakterisierung von G6PD-Mutanten [GPD-Mutanten]
Spectrophotometry assays to determine G6PD activity from Trinity Biotech and Pointe Scientific G6PD show good correlation
G6PD testing in support of treatment and elimination of malaria: recommendations for evaluation of G6PD tests
Neonatal Hyperbilirubinemia in infants with G6PD c.563C > T Variant
G6PD genetic variations in neonatal Hyperbilirubinemia in Indonesian Deutromalay population
Effect of neonatal reticulocytosis on glucose 6-phosphate dehydrogenase (G6PD) activity and G6PD deficiency detection: a cross-sectional study
Hemolytic crisis in a G6PD-deficient infant after ingestion of pumpkin
Charakterisierung und Vergleich von "Mittelmeer"- ähnlichen und (A-)- ähnlichen G6PD- Varianten, Charakterisierung einer G6PD- Variante einer G6PD- defekten Maus und Einsatz der Mikroimmunoaffinitätschromatografie zur Isolierung der G6PD
Molekulargenetische G6PD-Genotypisierung und Bestimmung er Genfrequenzen polymorpher G6PD-Varianten in Südwest-Nigeria
A novel G6PD deleterious variant identified in three families with severe glucose-6-phosphate dehydrogenase deficiency
Novel TRPV6 variant linked with transient neonatal hyperparathyroidism
Assessment of CareStart G6PD rapid diagnostic test and CareStart G6PD biosensor in Mauritania
Charakterisierung von G6PD-Mutanten [GPD-Mutanten]
Spectrophotometry assays to determine G6PD activity from Trinity Biotech and Pointe Scientific G6PD show good correlation