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Journal Abstract Search

141 related items for PubMed ID: 19795528

  • 1. 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; 20 Suppl 1():608-11. PubMed ID: 19795528
    [Abstract] [Full Text] [Related]

  • 2. Minor-form, microform, and mini-microform cleft lip: anatomical features, operative techniques, and revisions.
    Yuzuriha S, Mulliken JB.
    Plast Reconstr Surg; 2008 Nov; 122(5):1485-1493. PubMed ID: 18971733
    [Abstract] [Full Text] [Related]

  • 3. Asymmetrical bilateral cleft lip: complete or incomplete and contralateral lesser defect (minor-form, microform, or mini-microform).
    Yuzuriha S, Oh AK, Mulliken JB.
    Plast Reconstr Surg; 2008 Nov; 122(5):1494-1504. PubMed ID: 18971734
    [Abstract] [Full Text] [Related]

  • 4. 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; 79(2):148-52. PubMed ID: 25590586
    [Abstract] [Full Text] [Related]

  • 5. Confirmation of TFAP2A gene involvement in branchio-oculo-facial syndrome (BOFS) and report of temporal bone anomalies.
    Stoetzel C, Riehm S, Bennouna Greene V, Pelletier V, Vigneron J, Leheup B, Marion V, Hellé S, Danse JM, Thibault C, Moulinier L, Veillon F, Dollfus H.
    Am J Med Genet A; 2009 Oct; 149A(10):2141-6. PubMed ID: 19764023
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. [Genetic analysis of a Chinese pedigree affected with Branchio-oculo-facial syndrome and a literature review].
    Li K, Sun H, Guo Y, Sun G, Duan H, Kong X, Liu N.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Sep 10; 41(9):1084-1089. PubMed ID: 39217487
    [Abstract] [Full Text] [Related]

  • 8. Genotype-phenotype analysis of the branchio-oculo-facial syndrome.
    Milunsky JM, Maher TM, Zhao G, Wang Z, Mulliken JB, Chitayat D, Clemens M, Stalker HJ, Bauer M, Burch M, Chénier S, Cunningham ML, Drack AV, Janssens S, Karlea A, Klatt R, Kini U, Klein O, Lachmeijer AM, Megarbane A, Mendelsohn NJ, Meschino WS, Mortier GR, Parkash S, Ray CR, Roberts A, Roberts A, Reardon W, Schnur RE, Smith R, Splitt M, Tezcan K, Whiteford ML, Wong DA, Zori R, Lin AE.
    Am J Med Genet A; 2011 Jan 10; 155A(1):22-32. PubMed ID: 21204207
    [Abstract] [Full Text] [Related]

  • 9. TFAP2A mutations result in branchio-oculo-facial syndrome.
    Milunsky JM, Maher TA, Zhao G, Roberts AE, Stalker HJ, Zori RT, Burch MN, Clemens M, Mulliken JB, Smith R, Lin AE.
    Am J Hum Genet; 2008 May 10; 82(5):1171-7. PubMed ID: 18423521
    [Abstract] [Full Text] [Related]

  • 10. 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 10; 27(6):1412-4. PubMed ID: 27607113
    [Abstract] [Full Text] [Related]

  • 11. Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation.
    Günes N, Cengiz FB, Duman D, Dervişoğlu S, Tekin M, Tüysüz B.
    Genet Couns; 2014 Sep 10; 25(1):41-7. PubMed ID: 24783654
    [Abstract] [Full Text] [Related]

  • 12. Tfap2a-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage.
    Green RM, Feng W, Phang T, Fish JL, Li H, Spritz RA, Marcucio RS, Hooper J, Jamniczky H, Hallgrímsson B, Williams T.
    Dis Model Mech; 2015 Jan 10; 8(1):31-43. PubMed ID: 25381013
    [Abstract] [Full Text] [Related]

  • 13. Ocular anomalies in the branchio-oculo-facial syndrome.
    Su CS, O'Hagen SB, Sullivan TJ.
    Aust N Z J Ophthalmol; 1998 Feb 10; 26(1):43-6. PubMed ID: 9524030
    [Abstract] [Full Text] [Related]

  • 14. Branchio-oculo-facial syndrome (BOFS) and congenital heart defects.
    Rosa RF, Zen PR, Graziadio C, Paskulin GA.
    Arq Bras Cardiol; 2009 Feb 10; 92(2):e6-8, e33-5. PubMed ID: 19360235
    [Abstract] [Full Text] [Related]

  • 15.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Lin AE, Haldeman-Englert CR, Milunsky JM.
    ; 1993 Feb 10. PubMed ID: 21634087
    [Abstract] [Full Text] [Related]

  • 16. Craniofacial phenotype in the branchio-oculo-facial syndrome: four case reports.
    Galliani E, Burglen L, Kadlub N, Just W, Sznajer Y, de Villemeur TB, Soupre V, Picard A, Vazquez MP.
    Cleft Palate Craniofac J; 2012 May 10; 49(3):357-64. PubMed ID: 21539471
    [Abstract] [Full Text] [Related]

  • 17. [Branchio-oculo-facial syndrome].
    Frascari F, Bieth E, Galinier P, Just W, Mazereeuw-Hautier J.
    Ann Dermatol Venereol; 2012 May 10; 139(8-9):550-4. PubMed ID: 22963965
    [Abstract] [Full Text] [Related]

  • 18. Detection of orbicularis oris muscle defects in first degree relatives of cleft lip children using ultrasound.
    Mittal M, Maheshwari N, Ahlawat K, Sharma V, Sultan A, Chopra R.
    J Indian Soc Pedod Prev Dent; 2012 May 10; 30(3):237-41. PubMed ID: 23263428
    [Abstract] [Full Text] [Related]

  • 19. Clinical features of the microform cleft lip and the ultrastructural characteristics of the orbicularis oris muscle.
    Kim EK, Khang SK, Lee TJ, Kim TG.
    Cleft Palate Craniofac J; 2010 May 10; 47(3):297-302. PubMed ID: 19860522
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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