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Mapping genetic diversity with the GenomeIndia project.
Nat Genet. 2025 Apr;57(4):767-773. doi: 10.1038/s41588-025-02153-x.
Nat Genet. 2025.
PMID: 40200122
No abstract available.
Kernicterus caused by a rare genetic variant of Crigler-Najjar Syndrome (c.826G>C).
Agarwal S, Uk KK, Parameswaran AS, Saini L, Singh K.
Agarwal S, et al. Among authors: parameswaran as.
Indian J Pediatr. 2024 Dec;91(12):1316. doi: 10.1007/s12098-024-05288-7. Epub 2024 Oct 18.
Indian J Pediatr. 2024.
PMID: 39419956
No abstract available.
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Blaschkoid Presentation of Congenital Ichthyosiform Erythroderma with Novel ABCA12 Mutation.
Bhatia D, Waghmare P, Parameswaran AS, Singh S.
Bhatia D, et al. Among authors: parameswaran as.
Indian J Pediatr. 2025 Jun;92(6):672. doi: 10.1007/s12098-025-05543-5. Epub 2025 Apr 26.
Indian J Pediatr. 2025.
PMID: 40285913
No abstract available.
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Author Correction: Mapping genetic diversity with the GenomeIndia project.
Bhattacharyya C, Subramanian K, Uppili B, Biswas NK, Ramdas S, Tallapaka KB, Arvind P, Rupanagudi KV, Maitra A, Nagabandi T, De T, Singh K, Sharma P, Sharma N, Raghav SK, Prasad P, Soniya EV, Jaleel A, Nelson Sathi S, Joshi M, Joshi C, Lahiri M, Dixit S, Shashidhara LS, Senthil Kumar N, Lalhruaitluanga H, Nundanga L, Shivakumar V, Venkatasubramanian G, Rao NP, Ganie MA, Wani IA, Jha G, Dalal A, Bashyam MD, Varadwaj PK, Bs S, Simmhan Y, Jain C, Sundar D, Gupta I, Yadav P, Sinha H, Narayanan M, Raman K, Padinjat R, Sabarinathan R; GenomeIndia Consortium; Narahari Y, Ravindranath V, Thangaraj K, Sowpati DT, Faruq M, Basu A, Kahali B.
Bhattacharyya C, et al.
Nat Genet. 2025 Jun;57(6):1563. doi: 10.1038/s41588-025-02206-1.
Nat Genet. 2025.
PMID: 40341780
No abstract available.
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