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Journal Abstract Search

322 related items for PubMed ID: 30413887

  • 21. Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate.
    Sahoo T, Theisen A, Sanchez-Lara PA, Marble M, Schweitzer DN, Torchia BS, Lamb AN, Bejjani BA, Shaffer LG, Lacassie Y.
    Am J Med Genet A; 2011 Jul; 155A(7):1646-53. PubMed ID: 21671386
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  • 22. Deficiency of Fam20b-Catalyzed Glycosaminoglycan Chain Synthesis in Neural Crest Leads to Cleft Palate.
    Chen X, Li N, Hu P, Li L, Li D, Liu H, Zhu L, Xiao J, Liu C.
    Int J Mol Sci; 2023 Jun 01; 24(11):. PubMed ID: 37298583
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  • 23. Microdeletion del(22)(q12.2) encompassing the facial development-associated gene, MN1 (meningioma 1) in a child with Pierre-Robin sequence (including cleft palate) and neurofibromatosis 2 (NF2): a case report and review of the literature.
    Davidson TB, Sanchez-Lara PA, Randolph LM, Krieger MD, Wu SQ, Panigrahy A, Shimada H, Erdreich-Epstein A.
    BMC Med Genet; 2012 Mar 22; 13():19. PubMed ID: 22436304
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  • 24. Intraflagellar transport 88 (IFT88) is crucial for craniofacial development in mice and is a candidate gene for human cleft lip and palate.
    Tian H, Feng J, Li J, Ho TV, Yuan Y, Liu Y, Brindopke F, Figueiredo JC, Magee W, Sanchez-Lara PA, Chai Y.
    Hum Mol Genet; 2017 Mar 01; 26(5):860-872. PubMed ID: 28069795
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  • 29. Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface.
    Welsh IC, Hart J, Brown JM, Hansen K, Rocha Marques M, Aho RJ, Grishina I, Hurtado R, Herzlinger D, Ferretti E, Garcia-Garcia MJ, Selleri L.
    J Anat; 2018 Aug 01; 233(2):222-242. PubMed ID: 29797482
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  • 33. Mycn deficiency underlies the development of orofacial clefts in mice and humans.
    Yang R, Li R, Huang Z, Zuo Y, Yue H, Wu H, Gu F, Wang F, He M, Bian Z.
    Hum Mol Genet; 2022 Mar 03; 31(5):803-815. PubMed ID: 34590686
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