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Page 1
Acute Myeloid Leukemia and Next-Generation Sequencing Panels for Diagnosis: A Comprehensive Review.
J Pediatr Hematol Oncol. 2024 Apr 1;46(3):125-137. doi: 10.1097/MPH.0000000000002840. Epub 2024 Feb 29.
J Pediatr Hematol Oncol. 2024.
PMID: 38447075
Free PMC article.
Review.
Whole exome sequencing reveals rare variants linked to congenital pouch colon.
Mathur P, Medicherla KM, Chaudhary S, Patel M, Bagali P, Suravajhala P.
Mathur P, et al. Among authors: chaudhary s.
Sci Rep. 2018 Apr 27;8(1):6646. doi: 10.1038/s41598-018-24967-y.
Sci Rep. 2018.
PMID: 29703930
Free PMC article.
Item in Clipboard
Validation of a method for diosgenin extraction from fenugreek (Trigonella foenum-graecum L.).
Chaudhary SA, Chaudhary PS, Syed BA, Misra R, Bagali PG, Vitalini S, Iriti M.
Chaudhary SA, et al.
Acta Sci Pol Technol Aliment. 2018 Oct-Dec;17(4):377-385. doi: 10.17306/J.AFS.0606.
Acta Sci Pol Technol Aliment. 2018.
PMID: 30558394
Free article.
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Elicitation of Diosgenin Production in Trigonella foenum-graecum (Fenugreek) Seedlings by Methyl Jasmonate.
Chaudhary S, Chikara SK, Sharma MC, Chaudhary A, Alam Syed B, Chaudhary PS, Mehta A, Patel M, Ghosh A, Iriti M.
Chaudhary S, et al.
Int J Mol Sci. 2015 Dec 15;16(12):29889-99. doi: 10.3390/ijms161226208.
Int J Mol Sci. 2015.
PMID: 26694357
Free PMC article.
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Author Correction: Whole exome sequencing reveals rare variants linked to congenital pouch colon.
Mathur P, Medicherla KM, Chaudhary S, Patel M, Bagali P, Suravajhala P.
Mathur P, et al. Among authors: chaudhary s.
Sci Rep. 2018 Sep 11;8(1):13867. doi: 10.1038/s41598-018-32119-5.
Sci Rep. 2018.
PMID: 30206290
Free PMC article.
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Whole-Genome Sequencing of Brevundimonas diminuta XGC1, Isolated from a Tuberculosis Patient in Gujarat, India.
Ghosh A, Chandratre K, Chaudhary A, Chaudhary S, Badani N, Chaudhary PS, Dhawan D, Vudathala S, Chikara SK.
Ghosh A, et al. Among authors: chaudhary s.
Genome Announc. 2015 Jun 25;3(3):e00686-15. doi: 10.1128/genomeA.00686-15.
Genome Announc. 2015.
PMID: 26112790
Free PMC article.
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Compound heterozygous β(+) β(0) mutation of HBB gene leading to β-thalassemia major in a Gujarati family - A case study.
Chaudhary S, Dhawan D, Bagali PG, S Chaudhary P, Chaudhary A, Singh S, Vudathala S.
Chaudhary S, et al.
Mol Genet Metab Rep. 2016 Apr 13;7:51-3. doi: 10.1016/j.ymgmr.2016.04.002. eCollection 2016 Jun.
Mol Genet Metab Rep. 2016.
PMID: 27134826
Free PMC article.
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