- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Bibliographic citation
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Heterogeneous Presentation of Neonatal Hemochromatosis in Dichorionic Twins ; volume:08 ; number:04 ; year:2018 ; pages:e332-e334
AJP reports ; 08, Heft 04 (2018), e332-e334
- Contributor
-
Chee, Yee Yuet
Wong, Siu Chun Mabel
Wong, Ming Sum Rosanna
- DOI
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10.1055/s-0038-1675335
- URN
-
urn:nbn:de:101:1-2019041408280847504505
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:55 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
- Chee, Yee Yuet
- Wong, Siu Chun Mabel
- Wong, Ming Sum Rosanna
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Neonatal Hypopituitarism: Unusual Presentation
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Impact of HFEgenetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data
Preterm twins with antenatal presentation of Pearson syndrome
Neonatal hemochromatosis with εγδβ-thalassemia: a case report and analysis of serum iron regulators
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Molecular basis of HFE-hemochromatosis
An Unusual Neonatal Presentation of Scimitar Syndrome
2039 T2* CMR in hereditary hemochromatosis
Hepatic failure, neonatal hemochromatosis and porto-pulmonary hypertension in a newborn with trisomy 21 - a case report
Neonatal Hemochromatosis: A Congenital Alloimmune Hepatitis
Neonatal Hemochromatosis: Treatment with Exchange Transfusion and Intravenous Immunoglobulin
Neonatal Hypopituitarism: Unusual Presentation
Neonatal Lupus presenting with neonatal hemochromatosis-like liver disease that responded to steroids: a case report
Impact of HFEgenetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data
Preterm twins with antenatal presentation of Pearson syndrome
Neonatal hemochromatosis with εγδβ-thalassemia: a case report and analysis of serum iron regulators
Synovial immunopathology in hemochromatosis arthropathy
Molecular basis of HFE-hemochromatosis
An Unusual Neonatal Presentation of Scimitar Syndrome
2039 T2* CMR in hereditary hemochromatosis