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.


PUBMED FOR HANDHELDS

Journal Abstract Search


155 related items for PubMed ID: 1519658

  • 1. Beare-Stevenson cutis gyrata syndrome.
    Hall BD, Cadle RG, Golabi M, Morris CA, Cohen MM.
    Am J Med Genet; 1992 Sep 01; 44(1):82-9. PubMed ID: 1519658
    [Abstract] [Full Text] [Related]

  • 2. Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome.
    Przylepa KA, Paznekas W, Zhang M, Golabi M, Bias W, Bamshad MJ, Carey JC, Hall BD, Stevenson R, Orlow S, Cohen MM, Jabs EW.
    Nat Genet; 1996 Aug 01; 13(4):492-4. PubMed ID: 8696350
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Beare-Stevenson syndrome: two Dutch patients with cerebral abnormalities.
    Barge-Schaapveld DQ, Brooks AS, Lequin MH, van Spaendonk R, Vermeulen RJ, Cobben JM.
    Pediatr Neurol; 2011 Apr 01; 44(4):303-7. PubMed ID: 21397175
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. A severe case of Beare-Stevenson syndrome and associated congenital deformities.
    Andrews JM, Martins DM, Ramos RR, Ferreira LM.
    Br J Plast Surg; 1993 Jul 01; 46(5):443-6. PubMed ID: 8369884
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. A Case of Beare-Stevenson Syndrome with Unusual Manifestations.
    Ron N, Leung S, Carney E, Gerber A, David KL.
    Am J Case Rep; 2016 Apr 15; 17():254-8. PubMed ID: 27079505
    [Abstract] [Full Text] [Related]

  • 11. Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeve.
    Wenger TL, Bhoj EJ, Wetmore RF, Mennuti MT, Bartlett SP, Mollen TJ, McDonald-McGinn DM, Zackai EH.
    Am J Med Genet A; 2015 Apr 15; 167A(4):852-7. PubMed ID: 25706251
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. A case of Beare-Stevenson cutis gyrata syndrome confirmed by mutation analysis of the fibroblast growth factor receptor 2 gene.
    Akai T, Iizuka H, Kishibe M, Kawakami S, Kobayashi A, Ozawa T.
    Pediatr Neurosurg; 2002 Aug 15; 37(2):97-9. PubMed ID: 12145519
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis.
    Cohen MM.
    Am J Med Genet; 1993 Feb 01; 45(3):300-7. PubMed ID: 8434615
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Beare-Stevenson cutis gyrata syndrome with Chiari malformation.
    Wang TJ, Hung KS, Chen PK, Chuang WL, Shih TY, Lai BJ, Hsiao M.
    Acta Neurochir (Wien); 2002 Jul 01; 144(7):743-5. PubMed ID: 12181710
    [No Abstract] [Full Text] [Related]

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


    Page: [Next] [New Search]
    of 8.