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Page 1
Prenatal Diagnosis of a Heterotaxy Syndrome.
White A, Poorvu T, Estroff J, U Morton S, H Wojcik M. White A, et al. Among authors: poorvu t. Neoreviews. 2024 Sep 1;25(9):e594-e600. doi: 10.1542/neo.25-9-e594. Neoreviews. 2024. PMID: 39217136 No abstract available.
Caudal regression in fetus with de novo SMARCA2 pathogenic variant.
Wang MJ, Febres-Cordero DA, Poorvu T, Delerme P, Hecht J, Oyelese Y, O'Brien B, Ferrés MA. Wang MJ, et al. Among authors: poorvu t. Prenat Diagn. 2024 Aug;44(9):1111-1114. doi: 10.1002/pd.6627. Epub 2024 Jun 14. Prenat Diagn. 2024. PMID: 38877377
Genetic diagnosis in the fetus.
Wojcik MH, Reimers R, Poorvu T, Agrawal PB. Wojcik MH, et al. Among authors: poorvu t. J Perinatol. 2020 Jul;40(7):997-1006. doi: 10.1038/s41372-020-0627-z. Epub 2020 Feb 24. J Perinatol. 2020. PMID: 32094481 Free PMC article. Review.
Pregnant Women's Perspectives on Expanded Carrier Screening.
Propst L, Connor G, Hinton M, Poorvu T, Dungan J. Propst L, et al. Among authors: poorvu t. J Genet Couns. 2018 Sep;27(5):1148-1156. doi: 10.1007/s10897-018-0232-x. Epub 2018 Feb 23. J Genet Couns. 2018. PMID: 29476298