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

PUBMED FOR HANDHELDS

Journal Abstract Search

145 related items for PubMed ID: 4034800

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. Apert syndrome in a newborn infant without craniosynostosis.
    Coomaralingam S, Roth P.
    J Craniofac Surg; 2012 May; 23(3):e209-11. PubMed ID: 22627435
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. [The Apert syndrome (acrocephalosyndactylia). A case study].
    Flerow W, Szamak F.
    Fortschr Med; 1979 Mar 15; 97(10):438-9. PubMed ID: 422084
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. [On Apert syndrome. A case report].
    Vescuso A, Cicale F, De Martino A.
    Minerva Pediatr; 1993 Jun 15; 45(6):269-72. PubMed ID: 8232115
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Physical and oral characteristics of Crouzon syndrome, Apert syndrome, and Pierre Robin sequence.
    Horbelt CV.
    Gen Dent; 2008 Jun 15; 56(2):132-4. PubMed ID: 18348368
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. [FGFR2 gene mutation in a family with Crouzon syndrome and a sporadic Crouzon syndrome patient].
    Guo L, Lai YN, Li LX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Apr 15; 25(2):218-20. PubMed ID: 18393251
    [Abstract] [Full Text] [Related]

  • 40. Application of the three-dimensional maximum mode in prenatal diagnosis of Apert syndrome.
    Esser T, Rogalla P, Bamberg C, Kalache KD.
    Am J Obstet Gynecol; 2005 Nov 15; 193(5):1743-5. PubMed ID: 16260220
    [Abstract] [Full Text] [Related]

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