BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

405 related articles for article (PubMed ID: 8669439)

  • 41. [Anus-hand-ear syndrome (Townes-Brocks syndrome)].
    Kurosawa K
    Ryoikibetsu Shokogun Shirizu; 2001; (33):211-2. PubMed ID: 11462405
    [No Abstract]   [Full Text] [Related]  

  • 42. Silver's syndrome with unusual presentations.
    Kapoor KL; Ahmad S; Karihalu PL; Ishar K
    J Indian Med Assoc; 1984 Nov; 82(11):408-10. PubMed ID: 6543559
    [No Abstract]   [Full Text] [Related]  

  • 43. [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]  

  • 44. Clinical manifestations in 17 Greek patients with Goldenhar syndrome.
    Touliatou V; Fryssira H; Mavrou A; Kanavakis E; Kitsiou-Tzeli S
    Genet Couns; 2006; 17(3):359-70. PubMed ID: 17100205
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [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]  

  • 46. Adult diagnosis of Townes-Brocks syndrome with renal failure: Two related cases and review of literature.
    Beaudoux O; Lebre AS; Doco Fenzy M; Spodenkiewicz M; Canivet E; Colosio C; Poirsier C
    Am J Med Genet A; 2021 Mar; 185(3):937-944. PubMed ID: 33438842
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Townes-Brocks syndrome in an infant with translocation t (5;16).
    Serville F; Lacombe D; Saura R; Billeaud C; Sergent MP
    Genet Couns; 1993; 4(2):109-12. PubMed ID: 8357560
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Fryns syndrome--pre and postnatal diagnosis].
    Dix U; Beudt U; Langenbeck U
    Z Geburtshilfe Perinatol; 1991; 195(6):280-4. PubMed ID: 1776320
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Oto-mandibulo-facial dysostosis: a case report.
    Indushekar KR; Muhamad N
    J Indian Soc Pedod Prev Dent; 2000 Dec; 18(4):135-8. PubMed ID: 11601181
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Two coding single nucleotide polymorphisms in the SALL1 gene in Townes-Brocks syndrome: a case report and review of the literature.
    Liang Y; Shen D; Cai W
    J Pediatr Surg; 2008 Feb; 43(2):391-3. PubMed ID: 18280297
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Congenital facial neuropathy in oculoauriculovertebral dysplasia-hemifacial microsomia (Goldenhar-Gorlin syndrome).
    Aleksic S; Budzilovich G; Reuben R; Sekhar HC; Feigin I; Finegold M; Boal D; Tokita N; Converse JM
    Bull Los Angeles Neurol Soc; 1976 Apr; 41(2):68-77. PubMed ID: 1030652
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A family with dominant oculoauriculovertebral spectrum.
    Stoll C; Viville B; Treisser A; Gasser B
    Am J Med Genet; 1998 Jul; 78(4):345-9. PubMed ID: 9714437
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Townes-Brocks syndrome versus expanded spectrum hemifacial microsomia: review of eight patients and further evidence of a "hot spot" for mutation in the SALL1 gene.
    Keegan CE; Mulliken JB; Wu BL; Korf BR
    Genet Med; 2001; 3(4):310-3. PubMed ID: 11478532
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A patient with VACTERL association, amelia and hemifacial microsomia.
    Aftimos S; Winship I
    Clin Dysmorphol; 1999 Apr; 8(2):135-7. PubMed ID: 10319203
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Townes-Brocks syndrome.
    Priya ; Malhotra AK
    Indian Pediatr; 2004 Jul; 41(7):743. PubMed ID: 15297694
    [No Abstract]   [Full Text] [Related]  

  • 57. 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]  

  • 58. Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects.
    Kiefer SM; Ohlemiller KK; Yang J; McDill BW; Kohlhase J; Rauchman M
    Hum Mol Genet; 2003 Sep; 12(17):2221-7. PubMed ID: 12915476
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Phenotypic and genotypic aspects of Townes-Brock syndrome: case report of patient in southern Brazil with a new SALL1 hotspot region nonsense mutation.
    Liberalesso PBN; Cordeiro ML; Karuta SCV; Koladicz KRJ; Nitsche A; Zeigelboim BS; Raskin S; Rauchman M
    BMC Med Genet; 2017 Nov; 18(1):125. PubMed ID: 29110636
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Significance of epibulbar dermoids in childhood].
    Anton M; Rehůrek J; Holousová M
    Cesk Pediatr; 1983 Dec; 38(12):728-31. PubMed ID: 6661794
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.