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Wide spectrum of novel and rare hemoglobin variants in the multi‐ethnic Indian population: A review.
- Published in:
- International Journal of Laboratory Hematology, 2024, v. 46, n. 3, p. 434, doi. 10.1111/ijlh.14267
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- Publication type:
- Article
Molecular Heterogeneity of Hb H Disease in India.
- Published in:
- Thalassemia Reports, 2022, v. 12, n. 3, p. 73, doi. 10.3390/thalassrep12030012
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- Publication type:
- Article
Newborn Screening and Clinical Profile of Children With Sickle Cell Disease in a Tribal Area of Gujarat.
- Published in:
- Indian Pediatrics, 2022, v. 59, n. 3, p. 230, doi. 10.1007/s13312-022-2476-7
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- Article
Prevalence of globin gene modifiers encountered in fetuses during antenatal diagnosis of hemoglobinopathies.
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- International Journal of Laboratory Hematology, 2020, v. 42, n. 4, p. 482, doi. 10.1111/ijlh.13232
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- Publication type:
- Article
Multicenter Evaluation of HemoTypeSC as a Point-of-Care Sickle Cell Disease Rapid Diagnostic Test for Newborns and Adults Across India.
- Published in:
- 2020
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- Publication type:
- journal article
The spatial epidemiology of sickle-cell anaemia in India.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-36077-w
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- Publication type:
- Article
Genetic lesions in the UGT1A1 genes among Gilbert’s syndrome patients from India.
- Published in:
- Molecular Biology Reports, 2018, v. 45, n. 6, p. 2733, doi. 10.1007/s11033-018-4305-6
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- Publication type:
- Article
Potential involvement of ubiquitin‐proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell disease.
- Published in:
- British Journal of Haematology, 2018, v. 182, n. 4, p. 559, doi. 10.1111/bjh.15437
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- Publication type:
- Article
An Improved Osmotic Fragility Protocol for Screening of Beta Thalassaemia Carriers in Remote and Resource Limited Settings.
- Published in:
- Journal of Clinical & Diagnostic Research, 2018, v. 12, n. 7, p. 22, doi. 10.7860/JCDR/2018/32773.11825
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- Publication type:
- Article
Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults.
- Published in:
- Annals of Human Genetics, 2017, v. 81, n. 1, p. 11, doi. 10.1111/ahg.12179
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- Publication type:
- Article
Haemoglobinopathies in tribal populations of India.
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- Indian Journal of Medical Research, 2015, v. 141, n. 5, p. 505
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- Publication type:
- Article
Sickle cell disease in tribal populations in India.
- Published in:
- Indian Journal of Medical Research, 2015, v. 141, n. 5, p. 509
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- Publication type:
- Article
glucose-6-phosphate dehydrogenase (G6PD) deiciency among tribal populations of India - Country scenario.
- Published in:
- Indian Journal of Medical Research, 2015, v. 141, n. 5, p. 516
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- Publication type:
- Article
Prevalence of clinically relevant (TA)n UGT1A1 promoter alleles in Indian neonates.
- Published in:
- Current Science (00113891), 2013, v. 105, n. 4, p. 446
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- Publication type:
- Article
Diverse phenotypic expression of sickle cell hemoglobin C disease in an Indian family.
- Published in:
- 2011
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- Publication type:
- Letter
Glucose-6-phosphate dehydrogenase deficiency in India.
- Published in:
- 2004
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- Publication type:
- journal article
Symptomatic presentation of a sickle cell heterozygote: An evaluation of genetic factors.
- Published in:
- American Journal of Hematology, 2001, v. 66, n. 4, p. 307, doi. 10.1002/ajh.1066
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- Publication type:
- Article
Effect of α-thalassemia on sickle-cell anemia linked to the Arab-Indian haplotype in India.
- Published in:
- American Journal of Hematology, 1997, v. 55, n. 2, p. 104, doi. 10.1002/(SICI)1096-8652(199706)55:2<104::AID-AJH9>3.0.CO;2-X
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- Publication type:
- Article