BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 7152383)

  • 41. Radiological findings in the DOOR syndrome.
    Thomas PS; Nevin NC
    Ann Radiol (Paris); 1982 Jan; 25(1):54-8. PubMed ID: 7065610
    [No Abstract]   [Full Text] [Related]  

  • 42. Progressive synosteosis in Apert's syndrome (acrocephalosyndactyly), with a description of roentgenographic changes in the feet.
    Schauerte EW; St-Aubin PM
    Am J Roentgenol Radium Ther Nucl Med; 1966 May; 97(1):67-73. PubMed ID: 5938051
    [No Abstract]   [Full Text] [Related]  

  • 43. Apert's syndrome. Report of two cases in the Bantu.
    Schorn D; Vorster BJ; van Rooyen RJ
    S Afr Med J; 1972 Jan; 46(2):32-5. PubMed ID: 5058499
    [No Abstract]   [Full Text] [Related]  

  • 44. Deformities of the great toe in Apert's syndrome.
    Dell PC; Sheppard JE
    Clin Orthop Relat Res; 1981 Jun; (157):113-8. PubMed ID: 7249444
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Macrodactyly: report of eight cases of a rare anomaly.
    Kostakoglu N; Kayikcioglu A; Safak T; Ozcan G; Kecik A; Gursu G
    Turk J Pediatr; 1996; 38(1):73-9. PubMed ID: 8819624
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Tissue expansion for the treatment of complete syndactyly of the first web.
    Coombs CJ; Mutimer KL
    J Hand Surg Am; 1994 Nov; 19(6):968-72. PubMed ID: 7876497
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A case of a four-day-old male with Carpenter's syndrome with transposition of great arteries.
    Balci S; Haytoğlu T; Ozer S
    Turk J Pediatr; 1998; 40(3):461-6. PubMed ID: 9763914
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Apert's syndrome correlates with low fibroblast growth factor receptor activity in stenosed cranial sutures.
    Bresnick S; Schendel S
    J Craniofac Surg; 1998 Jan; 9(1):92-5. PubMed ID: 9558576
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D; Farriaux JP
    J Genet Hum; 1971 Dec; 19(4):299-316. PubMed ID: 5152131
    [No Abstract]   [Full Text] [Related]  

  • 50. Apert's syndrome.
    Hanieh A; David DJ
    Childs Nerv Syst; 1993 Aug; 9(5):289-91. PubMed ID: 8252521
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The elbow in syndromic craniosynostosis.
    Anderson PJ; Hall CM; Evans RD; Hayward RD; Jones BM
    J Craniofac Surg; 1998 May; 9(3):201-6. PubMed ID: 9693548
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The feet in Pfeiffer's syndrome.
    Anderson PJ; Hall CM; Evans RD; Jones BM; Hayward RD
    J Craniofac Surg; 1998 Jan; 9(1):83-7. PubMed ID: 9558574
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Infantile craniosynostosis: clinical, radiological, and surgical considerations based on 100 surgically treated cases.
    Giuffrè R; Vagnozzi R; Savino S
    Acta Neurochir (Wien); 1978; 44(1-2):49-67. PubMed ID: 726961
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Apert's syndrome--a type of acrocephalosyndactyly (a case report).
    Punwani DV; Purohit V; Irani SF; Kumta NB
    J Postgrad Med; 1979 Apr; 25(2):109-11. PubMed ID: 501671
    [No Abstract]   [Full Text] [Related]  

  • 55. [Acrocephalosyndactylia (Apert's syndrome). Case report].
    Latte MC; Locatelli L; Carcano G; Contursi R
    Pediatria (Napoli); 1978 Sep; 86(3):455-70. PubMed ID: 754166
    [No Abstract]   [Full Text] [Related]  

  • 56. Novel frame-shift mutations of GLI3 gene in non-syndromic postaxial polydactyly patients.
    Wang Z; Wang J; Li Y; Geng J; Fu Q; Xu Y; Shen Y
    Clin Chim Acta; 2014 Jun; 433():195-9. PubMed ID: 24667698
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
    Guttmacher AE
    Am J Med Genet; 1993 Apr; 46(2):219-22. PubMed ID: 8484413
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Apert's syndrome (acrocephalosyndactylia) in a 6-year-old girl].
    Krawczyński M; Socha J; Stańska M
    Pediatr Pol; 1974 Apr; 49(4):473-7. PubMed ID: 4827686
    [No Abstract]   [Full Text] [Related]  

  • 59. [Craniosynostosis: a review of 14 cases (author's transl)].
    Broseta J; Frontera-Izquierdo P; Barberá J; Barcia-Salorio JL
    An Esp Pediatr; 1977 Mar; 10(3):281-8. PubMed ID: 931197
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Radiological case of the month: Apert's syndrome.
    Gwinn JL
    Am J Dis Child; 1968 Apr; 115(4):469-70. PubMed ID: 5642349
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.