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Journal Abstract Search

405 related items for PubMed ID: 15479962

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  • 3. The genetic factors contributing to the risk of cleft lip-cleft palate and their clinical utility.
    Askarian S, Gholami M, Khalili-Tanha G, Tehrani NC, Joudi M, Khazaei M, Ferns GA, Hassanian SM, Avan A, Joodi M.
    Oral Maxillofac Surg; 2023 Jun; 27(2):177-186. PubMed ID: 35426585
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  • 10. Whole exome sequencing identifies mutations in 10% of patients with familial non-syndromic cleft lip and/or palate in genes mutated in well-known syndromes.
    Basha M, Demeer B, Revencu N, Helaers R, Theys S, Bou Saba S, Boute O, Devauchelle B, Francois G, Bayet B, Vikkula M.
    J Med Genet; 2018 Jul; 55(7):449-458. PubMed ID: 29500247
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  • 12. Orofacial clefting: update on the role of genetics.
    Ghassibe M, Bayet B, Revencu N, Desmyter L, Verellen-Dumoulin C, Gillerot Y, Deggouj N, Vanwijck R, Vikkula M, CL/P Study Group.
    B-ENT; 2006 Jul; 2 Suppl 4():20-4. PubMed ID: 17366841
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  • 14. Shared molecular networks in orofacial and neural tube development.
    Kousa YA, Mansour TA, Seada H, Matoo S, Schutte BC.
    Birth Defects Res; 2017 Jan 30; 109(2):169-179. PubMed ID: 27933721
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  • 17. The genetics and epigenetics of orofacial clefts.
    Spritz RA.
    Curr Opin Pediatr; 2001 Dec 30; 13(6):556-60. PubMed ID: 11753106
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  • 18. [Genetic variation of MSX1 has a sexual dimorphism in non syndromic cleft palate in the Chilean population].
    Blanco R, Jara L, Villaseca C, Palomino H, Carreño H.
    Rev Med Chil; 1998 Jul 30; 126(7):781-7. PubMed ID: 9830770
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  • 20. A Comprehensive Genetic Analysis of Slovenian Families with Multiple Cases of Orofacial Clefts Reveals Novel Variants in the Genes IRF6, GRHL3, and TBX22.
    Slavec L, Geršak K, Eberlinc A, Hovnik T, Lovrečić L, Mlinarič-Raščan I, Karas Kuželički N.
    Int J Mol Sci; 2023 Feb 21; 24(5):. PubMed ID: 36901693
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