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Journal Abstract Search

134 related items for PubMed ID: 19360235

  • 21.
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  • 22. Branchio-oculo-facial syndrome with valvular pulmonic stenosis.
    Kapoor S, Kapur N.
    Indian Pediatr; 2004 Nov; 41(11):1180-1. PubMed ID: 15591681
    [No Abstract] [Full Text] [Related]

  • 23. Branchio-oculo-facial syndrome.
    Kulkarni ML, Deshmukh S, Kumar A, Kulkarni PM.
    Indian J Pediatr; 2005 Aug; 72(8):701-3. PubMed ID: 16131778
    [Abstract] [Full Text] [Related]

  • 24. Early diagnosis of branchio-oculo-facial syndrome in a patient with inner ear malformation and mild ocular involvement.
    Lugli L, Just W, Genovese E, Palma S, Ferrari F, Percesepe A.
    Clin Dysmorphol; 2015 Jan; 24(1):17-20. PubMed ID: 25325184
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  • 26. Another case of preaxial polydactyly and white forelock in branchio-oculo-facial syndrome.
    McGaughran J.
    Clin Dysmorphol; 2001 Jan; 10(1):67-8. PubMed ID: 11152153
    [Abstract] [Full Text] [Related]

  • 27. A Rare Case of Branchio-oculo-facial Syndrome: Clinical and Histopathological Features.
    Iraji F, Shahbazi M, Abtahi-Naeini B, Asilian A, Shahmoradi Z, Bostakian A, Rajabi P, Kazemipour S.
    Adv Biomed Res; 2018 Jan; 7():145. PubMed ID: 30596055
    [Abstract] [Full Text] [Related]

  • 28. Bilateral dermal thymus of neck in branchio-oculo-facial syndrome.
    Hiroshi Furukawa, Satoru Sasaki, Eisuke Uchiyama, Kunihiro Kawashima, Yuhei Yamamoto.
    J Plast Reconstr Aesthet Surg; 2006 Jan; 59(12):1385-7. PubMed ID: 17113525
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  • 29.
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  • 30. 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; 33(2):100-6. PubMed ID: 22191992
    [Abstract] [Full Text] [Related]

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  • 33. Bilateral congenital cholesteatoma in branchio-oto-renal syndrome.
    Worley GA, Vats A, Harcourt J, Albert DM.
    J Laryngol Otol; 1999 Sep; 113(9):841-3. PubMed ID: 10664690
    [Abstract] [Full Text] [Related]

  • 34. Clinical presentation and the presence of hearing impairment in branchio-oculo-facial syndrome: a new mutation in the TFAP2A gene.
    Thomeer HG, Crins TT, Kamsteeg EJ, Buijsman W, Cruysberg JR, Knoers NV, Cremers CW.
    Ann Otol Rhinol Laryngol; 2010 Dec; 119(12):806-14. PubMed ID: 21250552
    [Abstract] [Full Text] [Related]

  • 35. Diagnostic and surgical challenge: middle ear dermoid cyst in 12 month old with branchio-oto-renal syndrome and multiple middle-ear congenital anomalies.
    Johnston DR, Whittemore K, Poe D, Robson CD, Perez-Atayde AR.
    Int J Pediatr Otorhinolaryngol; 2011 Oct; 75(10):1341-5. PubMed ID: 21868107
    [Abstract] [Full Text] [Related]

  • 36. Congenital unilateral facial nerve palsy as an unusual presentation of BOR syndrome.
    Jankauskienė A, Azukaitis K.
    Eur J Pediatr; 2013 Feb; 172(2):273-5. PubMed ID: 22837071
    [Abstract] [Full Text] [Related]

  • 37. Branchio-oculo-facial syndrome: broadening the spectrum.
    McCool M, Weaver DD.
    Am J Med Genet; 1994 Feb 15; 49(4):414-21. PubMed ID: 8160736
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  • 38.
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  • 39. Branchio-oculo-facial syndrome: case report.
    Lin JL, Chen PK.
    Changgeng Yi Xue Za Zhi; 1999 Mar 15; 22(1):128-32. PubMed ID: 10418222
    [Abstract] [Full Text] [Related]

  • 40. Branchio-oculo-facial syndrome with ectodermal parathyroid tissue.
    Verret DJ, Murray AD, Hobar PC.
    Otolaryngol Head Neck Surg; 2005 Dec 15; 133(6):983-4. PubMed ID: 16360526
    [No Abstract] [Full Text] [Related]

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