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Short Stature Syndromes: Case Series from India.
Panigrahi I, Kaur P, Chaudhry C, Shariq M, Naorem DD, Gowtham BC, Kaur A, Dayal D. Panigrahi I, et al. Among authors: chaudhry c. J Pediatr Genet. 2021 Apr 14;11(4):279-286. doi: 10.1055/s-0041-1726037. eCollection 2022 Dec. J Pediatr Genet. 2021. PMID: 36267864 Free PMC article.
Sotos syndrome in two children from India.
Panigrahi I, Chaudhry C. Panigrahi I, et al. Among authors: chaudhry c. Am J Med Genet A. 2020 Sep;182(9):2181-2183. doi: 10.1002/ajmg.a.61751. Epub 2020 Jul 17. Am J Med Genet A. 2020. PMID: 32677741
Indian child with novel variant in OFD1 gene.
Panigrahi I, Ahuja C, Chaudhry C. Panigrahi I, et al. Among authors: chaudhry c. Am J Med Genet A. 2020 Oct;182(10):2236-2238. doi: 10.1002/ajmg.a.61768. Epub 2020 Jul 17. Am J Med Genet A. 2020. PMID: 32677760
Wolf-Hirschhorn syndrome: A case series from India.
Chaudhry C, Kaur A, Panigrahi I, Kaur A. Chaudhry C, et al. 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
Fluctuating weakness: clue in the eyes!
Kaur A, Chaudhry C, Mehta A, Kaur A. Kaur A, et al. Among authors: chaudhry c. BMJ Case Rep. 2020 Dec 28;13(12):e239211. doi: 10.1136/bcr-2020-239211. BMJ Case Rep. 2020. PMID: 33372023 Free PMC article. No abstract available.
Ayme gripp syndrome in an Indian patient.
Chaudhry C, Kaur P, Srivastava P, Kaur A. Chaudhry C, et al. Am J Med Genet A. 2021 Apr;185(4):1312-1316. doi: 10.1002/ajmg.a.62053. Epub 2021 Jan 1. Am J Med Genet A. 2021. PMID: 33528093
55 results