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Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
Škorić-Milosavljević D, Lahrouchi N, Bosada FM, Dombrowsky G, Williams SG, Lesurf R, Tjong FVY, Walsh R, El Bouchikhi I, Breckpot J, Audain E, Ilgun A, Beekman L, Ratbi I, Strong A, Muenke M, Heide S, Muir AM, Hababa M, Cross L, Zhou D, Pastinen T; German Competence Network for Congenital Heart Defects; Zackai E, Atmani S, Ouldim K, Adadi N, Steindl K, Rauch A, Brook D, Wilsdon A, Kuipers I, Blom NA, Mulder BJ, Mefford HC, Keren B, Joset P, Kruszka P, Thiffault I, Sheppard SE, Roberts A, Lodder EM, Keavney BD, Clur SB, Mital S, Hitz MP, Christoffels VM, Postma AV, Bezzina CR. Škorić-Milosavljević D, et al. Among authors: atmani s. Genet Med. 2021 Oct;23(10):1952-1960. doi: 10.1038/s41436-021-01212-y. Epub 2021 Jun 10. Genet Med. 2021. PMID: 34113005 Free PMC article.
Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.
Škorić-Milosavljević D, Lahrouchi N, Bosada FM, Dombrowsky G, Williams SG, Lesurf R, Tjong FVY, Walsh R, El Bouchikhi I, Breckpot J, Audain E, Ilgun A, Beekman L, Ratbi I, Strong A, Muenke M, Heide S, Muir AM, Hababa M, Cross L, Zhou D, Pastinen T; German Competence Network for Congenital Heart Defects; Zackai E, Atmani S, Ouldim K, Adadi N, Steindl K, Rauch A, Brook D, Wilsdon A, Kuipers I, Blom NA, Mulder BJ, Mefford HC, Keren B, Joset P, Kruszka P, Thiffault I, Sheppard SE, Roberts A, Lodder EM, Keavney BD, Clur SB, Mital S, Hitz MP, Christoffels VM, Postma AV, Bezzina CR. Škorić-Milosavljević D, et al. Among authors: atmani s. Genet Med. 2021 Oct;23(10):2013. doi: 10.1038/s41436-021-01279-7. Genet Med. 2021. PMID: 34522030 Free PMC article. No abstract available.
Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects.
El Bouchikhi I, Bouguenouch L, Moufid FZ, Belhassan K, Samri I, Chaouti A, Houssaïni MI, Atmani S, Ouldim K. El Bouchikhi I, et al. Among authors: atmani s. Eurasian J Med. 2020 Oct;52(3):283-287. doi: 10.5152/eurasianjmed.2020.19237. Eurasian J Med. 2020. PMID: 33209082 Free PMC article.
Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate.
El Bouchikhi I, Belhassan K, Moufid FZ, Iraqui Houssaini M, Bouguenouch L, Samri I, Atmani S, Ouldim K. El Bouchikhi I, et al. Among authors: atmani s. Int J Pediatr Adolesc Med. 2016 Dec;3(4):133-142. doi: 10.1016/j.ijpam.2016.06.003. Epub 2016 Aug 18. Int J Pediatr Adolesc Med. 2016. PMID: 30805484 Free PMC article. Review.
[Apert syndrome].
Benmiloud S, Chaouki S, Atmani S, Hida M. Benmiloud S, et al. Among authors: atmani s. Pan Afr Med J. 2013;14:66. doi: 10.11604/pamj.2013.14.66.2178. Epub 2013 Feb 18. Pan Afr Med J. 2013. PMID: 23565313 Free PMC article. Review. French.
59 results