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

158 related items for PubMed ID: 6237297

  • 1. [Genetic study of children with congenital heart defects].
    Fäller K, Szollár J.
    Orv Hetil; 1984 Aug 19; 125(34):2071-5. PubMed ID: 6237297
    [No Abstract] [Full Text] [Related]

  • 2. Genetics of congenital heart diseases in syndromic and non-syndromic patients: new advances and clinical implications.
    Piacentini G, Digilio MC, Sarkozy A, Placidi S, Dallapiccola B, Marino B.
    J Cardiovasc Med (Hagerstown); 2007 Jan 19; 8(1):7-11. PubMed ID: 17255809
    [Abstract] [Full Text] [Related]

  • 3. Heritable syndromes with skeletal abnormalities and congenital heart disease.
    Martin EC.
    N Y State J Med; 1977 May 19; 77(6):944-50. PubMed ID: 140338
    [No Abstract] [Full Text] [Related]

  • 4. The Noonan-CFC controversy.
    Neri G, Zollino M, Reynolds JF.
    Am J Med Genet; 1991 Jun 01; 39(3):367-70. PubMed ID: 1867292
    [Abstract] [Full Text] [Related]

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

  • 6. Multiple pregnancy. 2.
    Benirschke K, Kim CK.
    N Engl J Med; 1973 Jun 21; 288(25):1329-36. PubMed ID: 4267537
    [No Abstract] [Full Text] [Related]

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

  • 8. Heart donors with underlying genetic syndromes.
    Gambino A, Torregrossa G, Feltrin G, Toscano G, Gerosa G.
    J Heart Lung Transplant; 2010 May 21; 29(5):588-9. PubMed ID: 20022768
    [No Abstract] [Full Text] [Related]

  • 9. Monozygotic Turner syndrome twins--correlation of phenotype severity and heart defect.
    Lin AE, Garver KL.
    Am J Med Genet; 1988 Mar 21; 29(3):529-31. PubMed ID: 3376996
    [Abstract] [Full Text] [Related]

  • 10. Retinitis pigmentosa in a young man with Noonan syndrome: further evidence that Noonan syndrome (NS) and the cardio-facio-cutaneous syndrome (CFC) are variable manifestations of the same entity?
    Lorenzetti ME, Fryns JP.
    Am J Med Genet; 1996 Oct 16; 65(2):97-9. PubMed ID: 8911596
    [Abstract] [Full Text] [Related]

  • 11. The genetics of congenital heart disease: a review of recent developments.
    Weismann CG, Gelb BD.
    Curr Opin Cardiol; 2007 May 16; 22(3):200-6. PubMed ID: 17413276
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 17. Genetic background of congenital conotruncal heart defects--a study of 45 families.
    Kwiatkowska J, Wierzba J, Aleszewicz-Baranowska J, Ereciński J.
    Kardiol Pol; 2007 Jan 16; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
    [Abstract] [Full Text] [Related]

  • 18. Chromosomal pattern, renal, cardiovascular and lymphatic abnormalities in a Nigerian child with Turner's syndrome and relative hypogamma-globulinaemia.
    Adeniyi A.
    West Afr Med J Niger Med Dent Pract; 1973 Dec 16; 22(6):93-6. PubMed ID: 4804898
    [No Abstract] [Full Text] [Related]

  • 19. [Cardiac malformations and genetic syndromes].
    Cardoso CR.
    Arq Bras Cardiol; 1983 Sep 16; 41(3):167-70. PubMed ID: 6232909
    [No Abstract] [Full Text] [Related]

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

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