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


166 related items for PubMed ID: 7438506

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

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

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

  • 4. Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosis.
    Canún S, Lomelí RM, Martínez R, Carnevale A.
    Clin Genet; 1984 Feb; 25(2):182-6. PubMed ID: 6705252
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No 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. Type A2 brachydactily: report of a new family.
    Rasore-Quartino A, Camera G.
    Acta Genet Med Gemellol (Roma); 1977 Feb; 26(2):141-50. PubMed ID: 596111
    [Abstract] [Full Text] [Related]

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

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

  • 16. Triphalangeal thumb and brachyectrodactyly syndrome: an uncommon entity with evidence of geographic distribution.
    Zenteno JC, Aguinaga M, Chávez V, Sastré N, Rivera MR, Kofman-Alfaro S.
    Clin Genet; 1996 Sep; 50(3):152-5. PubMed ID: 8946115
    [Abstract] [Full Text] [Related]

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

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

  • 19. Brachy/ectrodactyly and absence or hypoplasia of the fibula: an autosomal dominant condition with low penetrance and variable expressivity.
    Genuardi M, Zollino M, Bellussi A, Fuhrmann W, Neri G.
    Clin Genet; 1990 Nov; 38(5):321-6. PubMed ID: 2178076
    [Abstract] [Full Text] [Related]

  • 20. Congenital malformations of the limbs.
    da Fonseca LG, Freire-Maia N.
    Lancet; 1970 Jan 10; 1(7637):90-1. PubMed ID: 4188664
    [No Abstract] [Full Text] [Related]


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