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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2019 | 1 |
2020 | 1 |
2023 | 1 |
2024 | 0 |
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Genomics of rare genetic diseases-experiences from India.
Hum Genomics. 2019 Sep 25;14(1):52. doi: 10.1186/s40246-019-0215-5.
Hum Genomics. 2019.
PMID: 31554517
Free PMC article.
Review.
Autoinflammation and Myelofibrosis: Report of a Case.
Koduri PR, Shaik A, Vegulada DR.
Koduri PR, et al. Among authors: vegulada dr.
Turk J Haematol. 2023 Aug 31;40(3):223-224. doi: 10.4274/tjh.galenos.2023.2023.0064. Epub 2023 Jul 31.
Turk J Haematol. 2023.
PMID: 37519107
Free PMC article.
No abstract available.
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A case report of a novel 22 bp duplication within exon 1 of the UGT1A1 in a Sudanese infant with Crigler-Najjar syndrome type I.
Valmiki S, Mandapati KK, Miriyala LKV, Kelgeri CC, Rela M, Shanmugam NP, Vegulada DR.
Valmiki S, et al. Among authors: vegulada dr.
BMC Gastroenterol. 2020 Mar 6;20(1):62. doi: 10.1186/s12876-020-01192-4.
BMC Gastroenterol. 2020.
PMID: 32143638
Free PMC article.
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