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SHOX Variations in Idiopathic Short Stature in North India and a Review of Cases from Asian Countries.
Srivastava P, Tyagi A, Bamba C, Kumari A, Kaur H, Seth S, Kaur A, Panigrahi I, Dayal D, Pramanik S, Mandal K. Srivastava P, et al. Among authors: kaur a, kaur h. J Clin Res Pediatr Endocrinol. 2024 Mar 11;16(1):41-49. doi: 10.4274/jcrpe.galenos.2023.2023-3-13. Epub 2023 Sep 26. J Clin Res Pediatr Endocrinol. 2024. PMID: 37750395 Free PMC article. Review.
Gaucher disease: single gene molecular characterization of one-hundred Indian patients reveals novel variants and the most prevalent mutation.
Sheth J, Bhavsar R, Mistri M, Pancholi D, Bavdekar A, Dalal A, Ranganath P, Girisha KM, Shukla A, Phadke S, Puri R, Panigrahi I, Kaur A, Muranjan M, Goyal M, Ramadevi R, Shah R, Nampoothiri S, Danda S, Datar C, Kapoor S, Bhatwadekar S, Sheth F. Sheth J, et al. Among authors: kaur a. BMC Med Genet. 2019 Feb 14;20(1):31. doi: 10.1186/s12881-019-0759-1. BMC Med Genet. 2019. PMID: 30764785 Free PMC article.
Wolf-Hirschhorn syndrome: A case series from India.
Chaudhry C, Kaur A, Panigrahi I, Kaur A. Chaudhry C, et al. Among authors: kaur a. Am J Med Genet A. 2020 Dec;182(12):3048-3051. doi: 10.1002/ajmg.a.61856. Epub 2020 Sep 10. Am J Med Genet A. 2020. PMID: 32914558
It is in the face - Have a relook!
Endrakanti M, Kaur A, Panigrahi I, Pandiarajan V. Endrakanti M, et al. Among authors: kaur a. Neurol India. 2020 Sep-Oct;68(5):1244-1245. doi: 10.4103/0028-3886.299146. Neurol India. 2020. PMID: 33109891 Free article. No abstract available.
2,382 results