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Expanding the KIF4A-associated phenotype.
Kalantari S, Carlston C, Alsaleh N, Abdel-Salam GMH, Alkuraya F, Kato M, Matsumoto N, Miyatake S, Yamamoto T, Fares-Taie L, Rozet JM, Chassaing N, Vincent-Delorme C, Kang-Bellin A, McWalter K, Bupp C, Palen E, Wagner MD, Niceta M, Cesario C, Milone R, Kaplan J, Wadman E, Dobyns WB, Filges I. Kalantari S, et al. Am J Med Genet A. 2021 Dec;185(12):3728-3739. doi: 10.1002/ajmg.a.62443. Epub 2021 Aug 3. Am J Med Genet A. 2021. PMID: 34346154 Free PMC article.
Mosaic Williams syndrome: A case report.
Kalantari S, Biagio MD, Valente EM, Rossi E, Sirchia F. Kalantari S, et al. Am J Med Genet A. 2023 Jan;191(1):249-252. doi: 10.1002/ajmg.a.63002. Epub 2022 Oct 20. Am J Med Genet A. 2023. PMID: 36263864
A novel COLEC10 mutation in a child with 3MC syndrome.
Migliorero M, Kalantari S, Bracciamà V, Sorbini M, Arruga F, Peruzzi L, Biamino E, Amoroso A, Vaisitti T, Deaglio S. Migliorero M, et al. Among authors: kalantari s. Eur J Med Genet. 2021 Dec;64(12):104374. doi: 10.1016/j.ejmg.2021.104374. Epub 2021 Nov 2. Eur J Med Genet. 2021. PMID: 34740859
SIMPSON-GOLABI-BEHMEL syndrome type 1: How placental immunohistochemistry can rapidly Predict the diagnosis.
Fiandrino G, Arossa A, Ghirardello S, Kalantari S, Rossi C, Bonasoni MP, Cesari S, Rizzuti T, Giorgio E, Bassanese F, Scatigno AL, Meroni A, Melito C, Feltri M, Longo S, Figar TA, Andorno A, Gelli MC, Bertozzi M, Spinillo A, Riccipetitoni G, Valente EM, Paulli M, Sirchia F. Fiandrino G, et al. Among authors: kalantari s. Placenta. 2022 Aug;126:119-124. doi: 10.1016/j.placenta.2022.06.011. Epub 2022 Jun 30. Placenta. 2022. PMID: 35796063
Neoplasia in Cri du Chat Syndrome from Italian and German Databases.
Guala A, Spunton M, Kalantari S, Kennerknecht I, Danesino C. Guala A, et al. Among authors: kalantari s. Case Rep Genet. 2017;2017:5181624. doi: 10.1155/2017/5181624. Epub 2017 Apr 24. Case Rep Genet. 2017. PMID: 28523196 Free PMC article.
188 results