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Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations.
BMC Med Genet. 2020 Mar 12;21(1):50. doi: 10.1186/s12881-020-0986-5.
BMC Med Genet. 2020.
PMID: 32164556
Free PMC article.
Clinical, radiological and molecular studies in 24 individuals with Dyggve-Melchior-Clausen dysplasia and Smith-McCort dysplasia from India.
Varshney K, Narayanachar SG, Girisha KM, Bhavani GS, Narayanan D, Phadke S, Nampoothiri S, Udupi GA, Raghupathy P, Nair M, Geetha TS, Bhat M.
Varshney K, et al. Among authors: narayanachar sg.
J Med Genet. 2023 Feb;60(2):204-211. doi: 10.1136/jmedgenet-2021-108098. Epub 2022 Apr 27.
J Med Genet. 2023.
PMID: 35477554
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Molecular and clinical profiling in a large cohort of Asian Indians with glycogen storage disorders.
Kumar TV, Bhat M, Narayanachar SG, Narayan V, Srikanth AK, Anikar S, Shetty S.
Kumar TV, et al. Among authors: narayanachar sg.
PLoS One. 2022 Jul 14;17(7):e0270373. doi: 10.1371/journal.pone.0270373. eCollection 2022.
PLoS One. 2022.
PMID: 35834487
Free PMC article.
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