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

421 related items for PubMed ID: 2333896

  • 1. Autosomal dominant tibial hemimelia-polysyndactyly-triphalangeal thumbs syndrome: report of a Brazilian family.
    Richieri-Costa A, de Miranda E, Kamiya TY, Freire-Maia DV.
    Am J Med Genet; 1990 May; 36(1):1-6. PubMed ID: 2333896
    [Abstract] [Full Text] [Related]

  • 2. Syndactyly type IV/hexadactyly of feet associated with unilateral absence of the tibia.
    Rambaud-Cousson A, Dudin AA, Zuaiter AS, Thalji A.
    Am J Med Genet; 1991 Aug 01; 40(2):144-5. PubMed ID: 1654744
    [Abstract] [Full Text] [Related]

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

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

  • 5. Are triphalangeal thumb-polysyndactyly syndrome (TPTPS) and tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome (THPTTS) identical? A father with TPTPS and his daughter with THPTTS in a Thai family.
    Kantaputra PN, Chalidapong P.
    Am J Med Genet; 2000 Jul 17; 93(2):126-31. PubMed ID: 10869115
    [Abstract] [Full Text] [Related]

  • 6. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E, Goecke T, Meinecke P.
    Am J Med Genet; 1996 May 03; 63(1):185-9. PubMed ID: 8723107
    [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. Mirror image duplication of the hands and feet: report of a sporadic case with multiple congenital anomalies.
    Hersh JH, Dela Cruz TV, Pietrantoni M, von Drasek-Ascher G, Turnquest MA, Yacoub OA, Joyce MR.
    Am J Med Genet; 1995 Nov 20; 59(3):341-5. PubMed ID: 8599358
    [Abstract] [Full Text] [Related]

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

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

  • 15. Mutation of HOXA13 in hand-foot-genital syndrome.
    Mortlock DP, Innis JW.
    Nat Genet; 1997 Feb 20; 15(2):179-80. PubMed ID: 9020844
    [Abstract] [Full Text] [Related]

  • 16. Counseling dilemmas in EEC syndrome.
    Tekin M, Ohle C, Johnson DE, Christmas JT, Bodurtha J.
    Genet Couns; 2000 Feb 20; 11(1):19-24. PubMed ID: 10756423
    [Abstract] [Full Text] [Related]

  • 17. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L, Corsello G, Giuffrè M, Piccione M, Albanese A.
    Am J Med Genet; 1994 Jul 01; 51(3):266-9. PubMed ID: 8074157
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No 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 22.