Found: 15
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The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center.
- Published in:
- International Journal of Laboratory Hematology, 2019, v. 41, n. 2, p. 218, doi. 10.1111/ijlh.12948
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- Publication type:
- Article
Newborn screening for haemoglobinopathies by high performance liquid chromatography (HPLC): diagnostic utility of different approaches in resource-poor settings.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2014, v. 52, n. 12, p. 1791, doi. 10.1515/cclm-2014-0452
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- Publication type:
- Article
Variable phenotypes of sickle cell disease in India with the Arab- Indian haplotype.
- Published in:
- British Journal of Haematology, 2015, v. 168, n. 1, p. 156, doi. 10.1111/bjh.13083
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- Publication type:
- Article
Usefulness of automated chromatography for rapid fetal blood analysis for second trimester prenatal diagnosis of β-thalassemia.
- Published in:
- Prenatal Diagnosis, 2002, v. 22, n. 2, p. 153, doi. 10.1002/pd.251
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- Publication type:
- Article
Diverse phenotypes and transfusion requirements due to interaction of β-thalassemias with triplicated α-globin genes.
- Published in:
- 2015
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- Publication type:
- journal article
Effect of the Hemochromatosis Mutations on Iron Overload among the Indian β Thalassemia Carriers.
- Published in:
- 2017
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- Publication type:
- journal article
Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India.
- Published in:
- PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0147081
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- Publication type:
- Article
Exposure to Hydroxyurea During Pregnancy in Sickle-β Thalassemia: A Report of 2 Cases.
- Published in:
- 2010
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- Publication type:
- Case Study
Effect of Proinflammatory Cytokines (IL-6, TNF-α, and IL-1β) on Clinical Manifestations in Indian SLE Patients.
- Published in:
- Mediators of Inflammation, 2014, v. 2014, p. 1, doi. 10.1155/2014/385297
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- Publication type:
- Article
Congenital methemoglobinemia caused by Hb-MRatnagiri (-63CAT?TAT, His?Tyr) in an Indian family.
- Published in:
- American Journal of Hematology, 2005, v. 79, n. 2, p. 168, doi. 10.1002/ajh.20368
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- Publication type:
- Article
Alpha Genotyping in a Heterogeneous Indian Population.
- Published in:
- American Journal of Hematology, 1996, v. 53, n. 2, p. 149, doi. 10.1002/1096-8652(199610)53:2<149::AID-AJH2830530203>3.0.CO;2-H
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- Publication type:
- Article
Origin of the codon 47 (+A) β-thalassaemia mutation among the Nicobarese of the Andaman and Nicobar islands in India.
- Published in:
- 2007
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- Publication type:
- Letter
The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western India.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2015, v. 21, n. 2, p. 186, doi. 10.1177/1076029613495308
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- Publication type:
- Article
The fc receptor polymorphisms and expression of neutrophil activation markers in patients with sickle cell disease from Western India.
- Published in:
- 2013
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- Publication type:
- Journal Article
The Fc Receptor Polymorphisms and Expression of Neutrophil Activation Markers in Patients with Sickle Cell Disease from Western India.
- Published in:
- BioMed Research International, 2013, v. 2013, p. 1, doi. 10.1155/2013/457656
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- Publication type:
- Article