BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 11057204)

  • 21. Oculo-auriculo-vertebral spectrum with craniosynostosis and osteo-cartilagineous multiple defects: a diffuse chondro-membranous-osteo-dysplasia.
    Berio A; Garlaschi G; Mangiante G; Piazzi A
    Pediatr Med Chir; 2015 Dec; 37(3):pmc.2015.123. PubMed ID: 26714781
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Goldenhar syndrome associated with growth hormone deficiency.
    Yusufoğlu AM; Cetinkaya E; Ceylaner S; Aycan Z; Kibar E; Ekici F; Kizilgün M
    Genet Couns; 2008; 19(2):173-6. PubMed ID: 18618991
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Oculo-auriculo-vertebral spectrum disorder (Goldenhar "syndrome") coexisting with schizophreniform disorder.
    Brieger P; Bartel-Friedrich S; Haring A; Marneros A
    J Neurol Neurosurg Psychiatry; 1998 Jul; 65(1):135-6. PubMed ID: 9667580
    [No Abstract]   [Full Text] [Related]  

  • 24. Germinal mosaicism in oculo-auriculo-vertebral dysplasia?
    Lacombe D; Battin J
    Am J Med Genet; 1993 Jun; 46(5):609-10. PubMed ID: 8322831
    [No Abstract]   [Full Text] [Related]  

  • 25. Caruncle abnormalities in the oculo-auriculo-vertebral spectrum.
    Nijhawan N; Morad Y; Seigel-Bartelt J; Levin AV
    Am J Med Genet; 2002 Dec; 113(4):320-5. PubMed ID: 12457402
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of a case probably with Oral-Facial-Digital Syndrome--Gabrielli type.
    Güven MA; Ceylaner G; Ceylaner S; Uzel M; Coskun A
    Genet Couns; 2009; 20(2):167-72. PubMed ID: 19650414
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A case of oculo-auriculo-vertebral spectrum with long-term and comprehensive management.
    Suda N; Watanabe M; Ohyama K
    World J Orthod; 2006; 7(3):299-304. PubMed ID: 17009481
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Association of segmental neurofibromatosis 1 and oculo-auriculo-vertebral spectrum in a 24-year-old female.
    Castori M; Majore S; Romanelli F; Didona B; Grammatico P; Zambruno G
    Eur J Dermatol; 2008; 18(1):22-5. PubMed ID: 18086584
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Macrostomia: The defining feature of the oculo-auriculo-vertebral spectrum.
    Dutta M; Chatterjee I
    Acta Otorrinolaringol Esp (Engl Ed); 2019; 70(1):57-58. PubMed ID: 29728157
    [No Abstract]   [Full Text] [Related]  

  • 30. Oculo-auriculo-vertebral spectrum with myopathy and velopharyngeal insufficiency. A case report with a non-branchiomeric muscle biopsy.
    Murialdo G; Piazzi A; Badolati G; Calcagno E; Berio A
    Pediatr Med Chir; 2016 Jun; 38(2):121. PubMed ID: 27345603
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Multidisciplinary management of oculo-auriculo-vertebral spectrum.
    Vong A; Funamura J
    Curr Opin Otolaryngol Head Neck Surg; 2018 Aug; 26(4):234-241. PubMed ID: 29847352
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ultrasound diagnosis of oculo-auriculo-vertebral spectrum in a mid-trimester foetus.
    Song QY; Luo H
    Prenat Diagn; 2021 May; 41(6):791-792. PubMed ID: 33991116
    [No Abstract]   [Full Text] [Related]  

  • 33. [Goldenhar's oculo-auricular dysplasia].
    Mohieddine M
    Bull Soc Ophtalmol Fr; 1980 Oct; 80(10):957-9. PubMed ID: 7449018
    [No Abstract]   [Full Text] [Related]  

  • 34. Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case.
    Ng YY; Hu JM; Su PH; Chen JY; Yang MS; Chen SJ
    Acta Paediatr Taiwan; 2006; 47(3):142-5. PubMed ID: 17078468
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Diabetic mother's newborn with Goldenhar syndrome and cerebral malformations. Case report].
    Kerckoff Villanueva H; Retamoza B; Bautista A
    Ginecol Obstet Mex; 2008 Nov; 76(11):691-4. PubMed ID: 19065822
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Roberts-SC phocomelia syndrome].
    Kawame H
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):234-5. PubMed ID: 11057210
    [No Abstract]   [Full Text] [Related]  

  • 37. [Triploidy syndrome and diploid/triploid mixoploidy syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):361-2. PubMed ID: 11057261
    [No Abstract]   [Full Text] [Related]  

  • 38. TCOF1 mutations excluded from a role in other first and second branchial arch-related disorders.
    Splendore A; Passos-Bueno MR; Jabs EW; Van Maldergem L; Wulfsberg EA
    Am J Med Genet; 2002 Aug; 111(3):324-7. PubMed ID: 12210332
    [No Abstract]   [Full Text] [Related]  

  • 39. Goldenhar syndrome and hereditary tyrosinemia type 1.
    Al-Sayed MA; Asmari AM; Rashed MS
    Saudi Med J; 2002 Dec; 23(12):1527-31. PubMed ID: 12518207
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Oculoauriculovertebral spectrum in an infant of diabetic mother.
    Chen LT; Chang ML
    Acta Paediatr Taiwan; 2004; 45(6):346-9. PubMed ID: 15868852
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.