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

122 related items for PubMed ID: 9781029

  • 61.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 62. Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12.
    Ehtesham N, Cantor RM, King LM, Reinker K, Powell BR, Shanske A, Unger S, Rimoin DL, Cohn DH.
    Am J Hum Genet; 2002 Oct; 71(4):947-51. PubMed ID: 12161821
    [Abstract] [Full Text] [Related]

  • 63.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 64.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 65.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 66. Homozygosity mapping: familiarity breeds debility.
    Farrall M.
    Nat Genet; 1993 Oct; 5(2):107-8. PubMed ID: 8252033
    [No Abstract] [Full Text] [Related]

  • 67. A multiplex family with possible metaphyseal Spahr-type dysplasia and exclusion of RMRP and COL10A1 as candidate genes.
    Mégarbané A, Chouery E, Ghanem I.
    Am J Med Genet A; 2008 Jul 15; 146A(14):1865-70. PubMed ID: 18553549
    [Abstract] [Full Text] [Related]

  • 68.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 69.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 70.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 71.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 72.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 73. Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.
    Balemans W, Van Den Ende J, Freire Paes-Alves A, Dikkers FG, Willems PJ, Vanhoenacker F, de Almeida-Melo N, Alves CF, Stratakis CA, Hill SC, Van Hul W.
    Am J Hum Genet; 1999 Jun 15; 64(6):1661-9. PubMed ID: 10330353
    [Abstract] [Full Text] [Related]

  • 74. Pseudorheumatoid dysplasia. A rare genetic disorder simulating juvenile idiopathic arthritis.
    Duarte-Salazar C, Santillán-Chapa CG, Martínez-Coria E, Marin-Arriaga N, Miranda-Duarte A.
    Reumatol Clin; 2013 Jun 15; 9(5):316-8. PubMed ID: 23265789
    [Abstract] [Full Text] [Related]

  • 75.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 76.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 77.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 78.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 79. Progressive pseudorheumatoid dysplasia: a rare childhood disease.
    Torreggiani S, Torcoletti M, Campos-Xavier B, Baldo F, Agostoni C, Superti-Furga A, Filocamo G.
    Rheumatol Int; 2019 Mar 15; 39(3):441-452. PubMed ID: 30327864
    [Abstract] [Full Text] [Related]

  • 80.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.