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: 11822706

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

  • 2. The SPONASTRIME dysplasia: familial short-limb dwarfism with saddle nose, spinal alterations and metaphyseal striation. Report of 4 siblings.
    Fanconi S, Issler C, Giedion A, Prader A.
    Helv Paediatr Acta; 1983 Aug; 38(3):267-80. PubMed ID: 6618893
    [Abstract] [Full Text] [Related]

  • 3. SPONASTRIME dysplasia: report of an 11-year-old boy and review of the literature.
    Cooper HA, Crowe J, Butler MG.
    Am J Med Genet; 2000 May 01; 92(1):33-9. PubMed ID: 10797420
    [Abstract] [Full Text] [Related]

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

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Keratan sulphate excretion in a patient with Kniest dysplasia.
    Pennock CA, Gordon IR, Longdon K, Burman D.
    J Inherit Metab Dis; 1980 May 01; 2(3):75-8. PubMed ID: 6458738
    [Abstract] [Full Text] [Related]

  • 8. Sponastrime dysplasia. A radiologic-pathologic correlation.
    Lachman RS, Stoss H, Spranger J.
    Pediatr Radiol; 1989 May 01; 19(6-7):417-24. PubMed ID: 2771481
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Skeletal abnormalities in the Kniest syndrome with mucopolysacchariduria.
    Brill PW, Kim HJ, Beratis NG, Hirschhorn K.
    Am J Roentgenol Radium Ther Nucl Med; 1975 Nov 01; 125(3):731-8. PubMed ID: 128300
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Sponastrime dysplasia: five new cases and review of nine previously published cases.
    Langer LO, Beals RK, LaFranchi S, Scott CI, Sockalosky JJ.
    Am J Med Genet; 1996 May 03; 63(1):20-7. PubMed ID: 8723082
    [Abstract] [Full Text] [Related]

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

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

  • 15. Brachyolmia: an autosomal dominant form.
    Gardner J, Beighton P.
    Am J Med Genet; 1994 Feb 01; 49(3):308-12. PubMed ID: 8209891
    [Abstract] [Full Text] [Related]

  • 16. Changes in cat urinary glycosaminoglycans with age and in feline urologic syndrome.
    Pereira DA, Aguiar JA, Hagiwara MK, Michelacci YM.
    Biochim Biophys Acta; 2004 Apr 07; 1672(1):1-11. PubMed ID: 15056487
    [Abstract] [Full Text] [Related]

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

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

  • 19. [Metatropic dysplasia. A rare skeletal anomaly (author's transl)].
    Miething R, Stöver B, Noeske H.
    Monatsschr Kinderheilkd (1902); 1980 Mar 07; 128(3):153-6. PubMed ID: 7366584
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


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