BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 8322831)

  • 21. Facial asymmetries: problems in genetic counselling.
    Dodinval P
    J Genet Hum; 1979 Oct; 27(3):189-203. PubMed ID: 536738
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Oculo-auriculo-vertebral dysplasia. Presentation of a case and attempt at organizing the symptomatology].
    Salvitti C; Azulay RD; Heringer ML; Almeida de Faria IA
    AMB Rev Assoc Med Bras; 1978 May; 24(5):160-2. PubMed ID: 308674
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Autosomal dominant Goldenhar syndrome.
    Godel V; Regenbogen L; Goya V; Goodman RM
    Birth Defects Orig Artic Ser; 1982; 18(6):621-8. PubMed ID: 7171780
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. Goldenhar syndrome (oculo-auriculo-vertebral dysplasia): report of two cases.
    Ibhanesebhor SE
    East Afr Med J; 1995 May; 72(5):333-4. PubMed ID: 7555892
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Goldenhar complex with atypical associated anomalies: is the spectrum still widening?
    Konaş E; Canter HI; Mavili ME
    J Craniofac Surg; 2006 Jul; 17(4):669-72. PubMed ID: 16877912
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cardiovascular abnormalities in the oculo-auriculo-vertebral spectrum (Goldenhar syndrome).
    Morrison PJ; Mulholland HC; Craig BG; Nevin NC
    Am J Med Genet; 1992 Nov; 44(4):425-8. PubMed ID: 1442880
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Non-overlapping 22q11.2 microdeletions in patients with oculo-auriculo-vertebral spectrum.
    Dos Santos PA; de Oliveira SF; Freitas EL; Safatle HP; Rosenberg C; Ferrari I; Mazzeu JF
    Am J Med Genet A; 2014 Feb; 164A(2):551-3. PubMed ID: 24311469
    [No Abstract]   [Full Text] [Related]  

  • 32. [The etiology research progress of oculo-auriculo-vertebral spectrum].
    Wang P; Fan Y; Chen X
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Dec; 29(24):2184-8. PubMed ID: 27093828
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Familial occurrence of oculoauricolovertebral dysplasia and Franceschetti syndrome].
    Bestelmeyer U; Weerda H; Siegert R; Greiwe M; Schwinger E
    HNO; 1996 Aug; 44(8):452-5. PubMed ID: 8805011
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Goldenhar sequence and mosaic trisomy 22.
    Pridjian G; Gill WL; Shapira E
    Am J Med Genet; 1995 Dec; 59(4):411-3. PubMed ID: 8585556
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Syndrome with oculo dento auriculo cerebral malformation.
    Bhattacherjee H
    Indian J Ophthalmol; 1984; 32(3):185-6. PubMed ID: 6440861
    [No Abstract]   [Full Text] [Related]  

  • 36. New case of axial mesodermal dysplasia sequence: epidemiologic evidence of a single entity.
    Martínez-Frías ML; Gomar JL
    Am J Med Genet; 1994 Jan; 49(1):74-6. PubMed ID: 8172254
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Expanded spectrum of oculo-auriculo-vertebral spectrum with imperforate anus in a male patient who is negative for SALL1 mutations.
    Slavotinek AM; Vargervik K
    Clin Dysmorphol; 2011 Jan; 20(1):11-14. PubMed ID: 21188766
    [No Abstract]   [Full Text] [Related]  

  • 38. Hereditary hearing loss and ear dysplasia-renal adysplasia syndromes: syndrome delineation and possible pathogenesis.
    Melnick M
    Birth Defects Orig Artic Ser; 1980; 16(7):59-72. PubMed ID: 7213985
    [No Abstract]   [Full Text] [Related]  

  • 39. Malformations of the auricle: isolated and in syndromes. IV. Cumulative pedigree data.
    Kaye CI; Rollnick BR; Pruzansky S
    Birth Defects Orig Artic Ser; 1979; 15(5C):163-9. PubMed ID: 526600
    [No Abstract]   [Full Text] [Related]  

  • 40. Wide phenotypic variations within a family with SALL1 mutations: Isolated external ear abnormalities to Goldenhar syndrome.
    Kosaki R; Fujimaru R; Samejima H; Yamada H; Izumi K; Iijima K; Kosaki K
    Am J Med Genet A; 2007 May; 143A(10):1087-90. PubMed ID: 17431915
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.