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

280 related items for PubMed ID: 1481840

  • 1. Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorder.
    Kantaputra PN, Gorlin RJ, Langer LO.
    Am J Med Genet; 1992 Dec 01; 44(6):730-7. PubMed ID: 1481840
    [Abstract] [Full Text] [Related]

  • 2. [Familial mesomelial dwarfism (Nievergelt syndrome)].
    Hess OM, Goebel NH, Streuli R.
    Schweiz Med Wochenschr; 1978 Aug 05; 108(31):1202-6. PubMed ID: 675214
    [Abstract] [Full Text] [Related]

  • 3. A case of mesomelic dysplasia Kantaputra type--new findings and a new diagnostic approach.
    Siwicka KA, Kitoh H, Nishiyama M, Ishiguro N.
    J Pediatr Orthop B; 2008 Sep 05; 17(5):271-6. PubMed ID: 19471182
    [Abstract] [Full Text] [Related]

  • 4. [Tarsal-carpal coalition syndrome: a familial case].
    Caino S, Dello Ruso B, Fano V, Obregón MG.
    An Pediatr (Barc); 2012 Jun 05; 76(6):355-9. PubMed ID: 22326510
    [Abstract] [Full Text] [Related]

  • 5. [Distal symphalangia with humeroradial synostosis, carpal synostosis and brachyphalangia of the thumb. A dominant syndrome (author's transl)].
    Lenz W, Rehmann I.
    Z Orthop Ihre Grenzgeb; 1976 Apr 05; 114(2):202-11. PubMed ID: 1274395
    [Abstract] [Full Text] [Related]

  • 6. 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]

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

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Unilateral carpal bone deformity in mother and son.
    Krauss CM, Herman TE, Holmes LB.
    Am J Med Genet; 1987 Mar 01; 26(3):557-63. PubMed ID: 3565470
    [Abstract] [Full Text] [Related]

  • 10. Multiple synostosis syndrome: study of a large Brazilian kindred.
    da-Silva EO, Filho SM, de Albuquerque SC.
    Am J Med Genet; 1984 Jun 01; 18(2):237-47. PubMed ID: 6465200
    [Abstract] [Full Text] [Related]

  • 11. Kantaputra mesomelic dysplasia: a second reported family.
    Shears DJ, Offiah A, Rutland P, Sirimanna T, Bitner-Glindzicz M, Hall C.
    Am J Med Genet A; 2004 Jul 01; 128A(1):6-11. PubMed ID: 15211647
    [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. The multiple synostoses syndrome. A plea for simplicity.
    Nixon JR.
    Clin Orthop Relat Res; 1978 Sep 01; (135):48-51. PubMed ID: 709952
    [Abstract] [Full Text] [Related]

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

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

  • 18. [Congenital skeletal limb deficiencies. Examples and their treatment].
    Seyhan F, Ahiskali G.
    Turk Tip Cemiy Mecm; 1972 Nov 01; 38(11):481-8. PubMed ID: 4668355
    [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 14.