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

73 related items for PubMed ID: 2625625

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

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

  • 3. Familial third and fourth pharyngeal pouch syndrome with truncus arteriosus: DiGeorge syndrome.
    Raatikka M, Rapola J, Tuuteri L, Louhimo I, Savilahti E.
    Pediatrics; 1981 Feb; 67(2):173-5. PubMed ID: 7243440
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 7. Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis.
    De Koning TJ, Sandkuijl LA, De Schryver JE, Hennekam EA, Beemer FA, Houwen RH.
    Am J Med Genet; 1995 Jul 03; 57(3):479-82. PubMed ID: 7677155
    [Abstract] [Full Text] [Related]

  • 8. Familial duodenal atresia: a report of two families and review.
    Best LG, Wiseman NE, Chudley AE.
    Am J Med Genet; 1989 Nov 03; 34(3):442-4. PubMed ID: 2688422
    [Abstract] [Full Text] [Related]

  • 9. Nonsyndromal anencephaly: possible autosomal recessive variant.
    Farag TI, Teebi AS, Al-Awadi SA.
    Am J Med Genet; 1986 Jul 03; 24(3):461-4. PubMed ID: 3728564
    [Abstract] [Full Text] [Related]

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

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 13. [Hypermethioninemia. Apropos of a case in a consanguineous couple].
    Guízar Vázquez J, Sánchez Aguilar G, Velázquez A, Fragoso R, Rostenberg I, Alejandre I.
    Bol Med Hosp Infant Mex; 1980 Jul 03; 37(6):1237-44. PubMed ID: 7470271
    [Abstract] [Full Text] [Related]

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

  • 15. Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23.
    Stuhrmann M, Hennies HC, Bukhari IA, Brakensiek K, Nürnberg G, Becker C, Huebener J, Miranda MC, Frye-Boukhriss H, Knothe S, Schmidtke J, El-Harith EH.
    Clin Genet; 2008 Jun 03; 73(6):566-72. PubMed ID: 18462451
    [Abstract] [Full Text] [Related]

  • 16. [Familial Mediterranean fever with pseudodominant inheritance].
    Tarp BD, Obel N.
    Ugeskr Laeger; 2000 Nov 13; 162(46):6261-2. PubMed ID: 11107991
    [Abstract] [Full Text] [Related]

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

  • 18. Complete autologous reconstruction of the aorta and the pulmonary bifurcation in truncus arteriosus communis.
    Kaczmarek I, Schmauss D, Reichart B, Daebritz SH.
    Eur J Cardiothorac Surg; 2006 Oct 13; 30(4):675-7. PubMed ID: 16893652
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 4.