These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 27601832)

  • 1. Goldenhar Syndrome: A rare case report.
    Bhuyan R; Pati AR; Bhuyan SK; Nayak BB
    J Oral Maxillofac Pathol; 2016; 20(2):328. PubMed ID: 27601832
    [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. Maxillofacial features and systemic malformations in expanded spectrum Hemifacial Microsomia.
    Cohen N; Cohen E; Gaiero A; Zecca S; Fichera G; Baldi F; Giordanetto JF; Mercier JM; Cohen A
    Am J Med Genet A; 2017 May; 173(5):1208-1218. PubMed ID: 28319315
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Ipsilateral hemifacial microsomia with dextrocardia and pulmonary hypoplasia: A case report.
    Guo R; Chang SH; Wang BQ; Zhang QG
    World J Clin Cases; 2022 Mar; 10(9):2948-2953. PubMed ID: 35434090
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Hemifacial microsomia: skeletal abnormalities evaluation using CBCT (case report).
    Kabak SL; Savrasova NA; Zatochnaya VV; Melnichenko YM
    J Radiol Case Rep; 2019 Nov; 13(11):1-9. PubMed ID: 32190180
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. An Atypical Presentation of Goldenhar Syndrome With Seizures: A Rare Case Report.
    Tidke SC; Vagha JD; Vagha K; Lohiya S; Hampe P
    Cureus; 2023 Oct; 15(10):e46627. PubMed ID: 37936987
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Three-generation family with resemblance to Townes-Brocks syndrome and Goldenhar/oculoauriculovertebral spectrum.
    Johnson JP; Poskanzer LS; Sherman S
    Am J Med Genet; 1996 Jan; 61(2):134-9. PubMed ID: 8669439
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of hemifacial microsomia and ipsilateral cerebellar hypoplasia in a fetus with oculoauriculovertebral spectrum.
    Martinelli P; Maruotti GM; Agangi A; Mazzarelli LL; Bifulco G; Paladini D
    Ultrasound Obstet Gynecol; 2004 Aug; 24(2):199-201. PubMed ID: 15287060
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Goldenhar syndrome and hemifacial microsomia: observations on three patients.
    Thomas P
    Eur J Pediatr; 1980 May; 133(3):287-92. PubMed ID: 7389743
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 7q21.11 Microdeletion in a Neonate With Goldenhar Syndrome: Case Report and a Literature Review.
    Puvabanditsin S; February M; Francois L; Garrow E; Bruno C; Mehta R
    Cleft Palate Craniofac J; 2016 Mar; 53(2):249-52. PubMed ID: 26068384
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Oculoauriculovertebral spectrum with radial anomaly in child.
    Taksande A; Vilhekar K
    J Family Med Prim Care; 2013 Jan; 2(1):92-4. PubMed ID: 24479055
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital trigeminal neuropathy in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome).
    Aleksic S; Budzilovich G; Reuben R; Feigin I; Finegold M; McCarthy J; Aston S; Converse JM
    J Neurol Neurosurg Psychiatry; 1975 Oct; 38(10):1033-5. PubMed ID: 53276
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hemifacial Microsomia : Clinicoradiological Insight and Report of a Case.
    Chhabra N; Chhabra A
    Ethiop J Health Sci; 2017 Jan; 27(1):91-94. PubMed ID: 28458495
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Treatment of otological features of the oculoauriculovertebral dysplasia (Goldenhar syndrome).
    Skarzyński H; Porowski M; Podskarbi-Fayette R
    Int J Pediatr Otorhinolaryngol; 2009 Jul; 73(7):915-21. PubMed ID: 19203801
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.