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Year Number of Results
2019 5
2020 7
2021 7
2022 9
2023 13
2024 3

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33 results

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Page 1
Assisted reproductive technology: Short- and long-term outcomes.
Graham ME, Jelin A, Hoon AH Jr, Wilms Floet AM, Levey E, Graham EM. Graham ME, et al. Dev Med Child Neurol. 2023 Jan;65(1):38-49. doi: 10.1111/dmcn.15332. Epub 2022 Jul 18. Dev Med Child Neurol. 2023. PMID: 35851656 Free PMC article. Review.
Renal agenesis.
Society for Maternal-Fetal Medicine (SMFM); Jelin A. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2021 Nov;225(5):B28-B30. doi: 10.1016/j.ajog.2021.06.048. Epub 2021 Sep 8. Am J Obstet Gynecol. 2021. PMID: 34507792 No abstract available.
Prenatal Genetic Testing Options.
Jelin AC, Sagaser KG, Wilkins-Haug L. Jelin AC, et al. Pediatr Clin North Am. 2019 Apr;66(2):281-293. doi: 10.1016/j.pcl.2018.12.016. Pediatr Clin North Am. 2019. PMID: 30819336 Review.
Fetal CHD and perinatal outcomes.
Ge CJ, Mahle AC, Burd I, Jelin EB, Sekar P, Jelin AC. Ge CJ, et al. Cardiol Young. 2020 May;30(5):686-691. doi: 10.1017/S1047951120000785. Epub 2020 Apr 20. Cardiol Young. 2020. PMID: 32308170 Free PMC article.
The genetic etiologies of bilateral renal agenesis.
Kirschen GW, Blakemore K, Al-Kouatly HB, Fridkis G, Baschat A, Gearhart J, Jelin AC. Kirschen GW, et al. Prenat Diagn. 2024 Feb;44(2):205-221. doi: 10.1002/pd.6516. Epub 2024 Jan 5. Prenat Diagn. 2024. PMID: 38180355 Review.
Maternal implications of placental transfusion.
Uribe K, Chiruvolu A, Jelin AC. Uribe K, et al. Semin Perinatol. 2023 Jun;47(4):151733. doi: 10.1016/j.semperi.2023.151733. Epub 2023 Mar 17. Semin Perinatol. 2023. PMID: 37068968
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series.
Brar BK, Thompson MG, Vora NL, Gilmore K, Blakemore K, Miller KA, Giordano J, Dufke A, Wong B, Stover S, Lianoglou B, Van den Veyver I, Dempsey E, Rosner M, Chong K, Chitayat D, Sparks TN, Norton ME, Wapner R, Baranano K, Jelin AC; Fetal Sequencing Consortium. Brar BK, et al. Prenat Diagn. 2022 Dec;42(13):1686-1693. doi: 10.1002/pd.6269. Epub 2022 Nov 28. Prenat Diagn. 2022. PMID: 36403095 Free PMC article. Review.
Prenatal phenotype of 47, XXY (Klinefelter syndrome).
Swanson K, Bishop JC, Al-Kouatly HB, Makhamreh M, Felton T, Vora NL, Sparks TN, Jelin AC. Swanson K, et al. Prenat Diagn. 2023 Feb;43(2):207-212. doi: 10.1002/pd.6071. Epub 2021 Dec 7. Prenat Diagn. 2023. PMID: 34874073 Free PMC article. Review.
33 results