BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

174 related articles for article (PubMed ID: 25178617)

  • 1. Goldenhar syndrome - a case report.
    Mutanabbi M; Rahman MA; Mamun AA; Helal MA; Billah MB; Islam KA
    Mymensingh Med J; 2014 Jul; 23(3):586-9. PubMed ID: 25178617
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Thrombophilia gene mutations in oculoauriculovertebral spectrum.
    Tug E; Atasoy HI; Koybasi Sanal S
    Genet Couns; 2012; 23(1):65-72. PubMed ID: 22611644
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Oculo-auriculo-vertebral spectrum: clinical and molecular analysis of 51 patients.
    Beleza-Meireles A; Hart R; Clayton-Smith J; Oliveira R; Reis CF; Venâncio M; Ramos F; Sá J; Ramos L; Cunha E; Pires LM; Carreira IM; Scholey R; Wright R; Urquhart JE; Briggs TA; Kerr B; Kingston H; Metcalfe K; Donnai D; Newman WG; Saraiva JM; Tassabehji M
    Eur J Med Genet; 2015 Sep; 58(9):455-65. PubMed ID: 26206081
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical care in craniofacial microsomia: a review of current management recommendations and opportunities to advance research.
    Heike CL; Hing AV; Aspinall CA; Bartlett SP; Birgfeld CB; Drake AF; Pimenta LA; Sie KC; Urata MM; Vivaldi D; Luquetti DV
    Am J Med Genet C Semin Med Genet; 2013 Nov; 163C(4):271-82. PubMed ID: 24132932
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Goldenhar Syndrome - ophthalmologist's perspective.
    Schmitzer S; Burcel M; Dăscălescu D; Popteanu IC
    Rom J Ophthalmol; 2018; 62(2):96-104. PubMed ID: 30206552
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant microtia and ocular coloboma: new syndrome or an extension of the oculo-auriculo-vertebral spectrum?
    Beck AE; Hudgins L; Hoyme HE
    Am J Med Genet A; 2005 May; 134(4):359-62. PubMed ID: 15800906
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Craniofacial Microsomia: Goldenhar Syndrome in Association with Bilateral Congenital Cataract.
    Shrestha UD; Adhikari S
    Case Rep Ophthalmol Med; 2015; 2015():435967. PubMed ID: 26635984
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Limbal dermoid and Goldenhar syndrome. Report of an anatomoclinical study].
    D'Hermies F; Saragoussi JJ; Meyer A; Morel X; Fayet B; Dighiero P; Than-Trong T; Halhal M; Vu TA; Elmaleh C; Renard G
    J Fr Ophtalmol; 2001 Oct; 24(8):893-6. PubMed ID: 11894543
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Branchial cleft anomaly, congenital heart disease, and biliary atresia: Goldenhar complex or Lambert syndrome?
    Cohen J; Schanen NC
    Genet Couns; 2000; 11(2):153-6. PubMed ID: 10893666
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ocular findings in the facioauriculovertebral sequence (Goldenhar-Gorlin syndrome).
    Mansour AM; Wang F; Henkind P; Goldberg R; Shprintzen R
    Am J Ophthalmol; 1985 Oct; 100(4):555-9. PubMed ID: 4050929
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Goldenhar syndrome. Report of a new case].
    Pedraz García C; Benito Zaballos MF; García González P; Carbajosa Herrero T; Heras de Pedro M; Santos Borbujo J; Gil Sánchez A; Salazar Villalobos V
    An Esp Pediatr; 1984 Mar; 20(4):403-7. PubMed ID: 6732067
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical features of 149 patients with facio-auriculo-vertebral spectrum.
    Muñoz-Pedroza LA; Arenas-Sordo ML
    Acta Otorrinolaringol Esp; 2013; 64(5):359-62. PubMed ID: 23896491
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prenatal diagnosis of Goldenhar syndrome with unusual features by 3D ultrasonography.
    Guzelmansur I; Ceylaner G; Ceylaner S; Ceylan N; Daplan T
    Genet Couns; 2013; 24(3):319-25. PubMed ID: 24341148
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ocular motility disturbances (Duane retraction syndrome and double elevator palsy) with congenital heart disease, a rare association with Goldenhar syndrome--a case report.
    Verma MJ; Faridi MM
    Indian J Ophthalmol; 1992; 40(2):61-2. PubMed ID: 1452286
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): clinical, neuroradiologic, audiologic and cytogenetic findings.
    Engiz O; Balci S; Unsal M; Ozer S; Oguz KK; Aktas D
    Genet Couns; 2007; 18(3):277-88. PubMed ID: 18019368
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Goldenhar syndrome: ocular features.
    Bhallil S; Benatiya I; El Abdouni O; Mahjoubi B; Hicham T
    Bull Soc Belge Ophtalmol; 2010; (316):17-9. PubMed ID: 21305808
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Goldenhar syndrome in adults].
    Mitu F; Voloşciuc M; Mitu M; Arsenescu C; Arhire O; Pandele GI; Covic M
    Rev Med Chir Soc Med Nat Iasi; 2000; 104(3):127-32. PubMed ID: 12089913
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lipodermoid Cyst: A Report of a Rare Caruncular Case.
    Rajabi MT; Ramezani K
    Middle East Afr J Ophthalmol; 2015; 22(4):528-30. PubMed ID: 26692732
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Goldenhar syndrome in an infant of diabetic mother.
    Gharehbaghi MM; Ghaemi MR
    Iran J Pediatr; 2010 Mar; 20(1):131-4. PubMed ID: 23056696
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Goldenhar syndrome with limbal neoformation, microtia and skeletal deformities: a case report and literature review.
    Fu Y; Yu H; Zhang J; Zhou N
    BMC Ophthalmol; 2024 Feb; 24(1):81. PubMed ID: 38388885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.