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Journal Abstract Search

154 related items for PubMed ID: 21204207

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  • 3. A novel TFAP2A mutation in familial Branchio-Oculo-Facial Syndrome with predominant ocular phenotype.
    Aliferis K, Stoetzel C, Pelletier V, Hellé S, Angioï-Duprez K, Vigneron J, Leheup B, Marion V, Dollfus H.
    Ophthalmic Genet; 2011 Nov; 32(4):250-5. PubMed ID: 21728810
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  • 4. Analysis of TFAP2A mutations in Branchio-Oculo-Facial Syndrome indicates functional complexity within the AP-2α DNA-binding domain.
    Li H, Sheridan R, Williams T.
    Hum Mol Genet; 2013 Aug 15; 22(16):3195-206. PubMed ID: 23578821
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  • 6. A clinical and molecular analysis of branchio-oculo-facial syndrome patients in Russia revealed new mutations in TFAP2A.
    Meshcheryakova TI, Zinchenko RA, Vasilyeva TA, Marakhonov AV, Zhylina SS, Petrova NV, Kozhanova TV, Belenikin MS, Petrin AN, Mutovin GR.
    Ann Hum Genet; 2015 Mar 15; 79(2):148-52. PubMed ID: 25590586
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  • 7. A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene.
    Dumitrescu AV, Milunsky JM, Longmuir SQ, Drack AV.
    Ophthalmic Genet; 2012 Jun 15; 33(2):100-6. PubMed ID: 22191992
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  • 9. Additional clinical and molecular analyses of TFAP2A in patients with the branchio-oculo-facial syndrome.
    Reiber J, Sznajer Y, Posteguillo EG, Müller D, Lyonnet S, Baumann C, Just W.
    Am J Med Genet A; 2010 Apr 15; 152A(4):994-9. PubMed ID: 20358615
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  • 15. Lesser forms of cleft lip associated with the branchio-oculo-facial syndrome.
    Lin AE, Yuzuriha S, McLean S, Mulliken JB.
    J Craniofac Surg; 2009 Mar 15; 20 Suppl 1():608-11. PubMed ID: 19795528
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  • 18. An Unconventional Presentation of Branchio-Oculo-Facial Syndrome.
    Yi S, Albino FP, Wood BC, Sauerhammer TM, Rogers GF, Oh AK.
    J Craniofac Surg; 2016 Sep 15; 27(6):1412-4. PubMed ID: 27607113
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