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

165 related items for PubMed ID: 15379328

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [Association of the genetic variation of (MSX1-7) and non syndromic cleft lip palate in Chilean subjects].
    Blanco R, Jara L, Villaseca MC.
    Rev Med Chil; 1998 Jun; 126(6):637-45. PubMed ID: 9778871
    [Abstract] [Full Text] [Related]

  • 4. MSX1 and TGFB3 contribute to clefting in South America.
    Vieira AR, Orioli IM, Castilla EE, Cooper ME, Marazita ML, Murray JC.
    J Dent Res; 2003 Apr; 82(4):289-92. PubMed ID: 12651933
    [Abstract] [Full Text] [Related]

  • 5. [Genetic variation of MSX1 has a sexual dimorphism in non syndromic cleft palate in the Chilean population].
    Blanco R, Jara L, Villaseca C, Palomino H, Carreño H.
    Rev Med Chil; 1998 Jul; 126(7):781-7. PubMed ID: 9830770
    [Abstract] [Full Text] [Related]

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

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

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. [Association of muscle segment homeobox gene 1 polymorphisms with nonsyndromic cleft lip with or without cleft palate].
    Zhang L, Tang JL, Liang SZ.
    Hua Xi Kou Qiang Yi Xue Za Zhi; 2008 Jun; 26(3):256-7, 261. PubMed ID: 18705505
    [Abstract] [Full Text] [Related]

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

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 15. Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.
    Lidral AC, Romitti PA, Basart AM, Doetschman T, Leysens NJ, Daack-Hirsch S, Semina EV, Johnson LR, Machida J, Burds A, Parnell TJ, Rubenstein JL, Murray JC.
    Am J Hum Genet; 1998 Aug; 63(2):557-68. PubMed ID: 9683588
    [Abstract] [Full Text] [Related]

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

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 19. MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.
    van den Boogaard MJ, Dorland M, Beemer FA, van Amstel HK.
    Nat Genet; 2000 Apr; 24(4):342-3. PubMed ID: 10742093
    [No Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 9.