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


116 related items for PubMed ID: 5173224

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44. An unusual limb deformity in an inbred community.
    Mahloudji M, Farpour H.
    Birth Defects Orig Artic Ser; 1974; 10(5):75-80. PubMed ID: 4469998
    [No Abstract] [Full Text] [Related]

  • 45.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 46. The facio-audio-symphalangism syndrome: report of a case and review of the literature.
    Hurvitz SA, Goodman RM, Hertz M, Katznelson MB, Sack Y.
    Clin Genet; 1985 Jul; 28(1):61-8. PubMed ID: 4028502
    [Abstract] [Full Text] [Related]

  • 47. Robin sequence and oligodactyly in mother and son.
    Robinow M, Johnson GF, Apesos J.
    Am J Med Genet; 1986 Oct; 25(2):293-7. PubMed ID: 3777025
    [Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49. A malformation complex of ectrodactyly, clefting and hypomelanosis of ito (incontinentia pigmenti achromians).
    Stewart RE, Funderburk S, Setoguchi Y.
    Cleft Palate J; 1979 Oct; 16(4):358-62. PubMed ID: 290427
    [Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51. [The EEC or Rüdinger syndrome. Presentation of a case and orthopedic treatment].
    Frediani P, Zaltron D.
    Chir Organi Mov; 1980 Oct; 66(5):431-8. PubMed ID: 7344850
    [No Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53. The Roberts syndrome.
    Freeman MV, Williams DW, Schimke RN, Temtamy SA, Vachier E, German J.
    Birth Defects Orig Artic Ser; 1974 Oct; 10(5):87-95. PubMed ID: 4220010
    [Abstract] [Full Text] [Related]

  • 54.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 55.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 56.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58. [Congenital malformations caused by fimbriopathy. Case reports].
    Colombo ML, Magnetti L.
    Minerva Pediatr; 1982 Sep 30; 34(18):757-60. PubMed ID: 7144716
    [No Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 60.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 6.