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

64 related items for PubMed ID: 1057954

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

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [Clinical variations in Léri-Weill dyschondrosteosis].
    Duro EA, Prado GS.
    An Esp Pediatr; 1990 Nov; 33(5):461-3. PubMed ID: 2096761
    [Abstract] [Full Text] [Related]

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

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

  • 6. [Another case of dyschondrosteosis (Léri-Weill)].
    Becker PE.
    Humangenetik; 1965 Nov; 1(6):563-70. PubMed ID: 5868432
    [No Abstract] [Full Text] [Related]

  • 7. Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.
    Mutesa L, Vanbellinghen JF, Hellin AC, Segers K, Jamar M, Pierquin G, Bours V.
    Genet Couns; 2009 Nov; 20(1):9-17. PubMed ID: 19400538
    [Abstract] [Full Text] [Related]

  • 8. SHOX mutations in dyschondrosteosis (Leri-Weill syndrome).
    Belin V, Cusin V, Viot G, Girlich D, Toutain A, Moncla A, Vekemans M, Le Merrer M, Munnich A, Cormier-Daire V.
    Nat Genet; 1998 May; 19(1):67-9. PubMed ID: 9590292
    [Abstract] [Full Text] [Related]

  • 9. Radiographic patterns of dyschondrosteosis. (Leri-Weill disease).
    Hoeffel JC, Brauer B, Jimenez J, Hoeffel F.
    Radiol Clin Biol; 1973 May; 42(5):366-72. PubMed ID: 4745065
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Dyschondrosteose. Mesomelic dwarfism of Lwei and Weill.
    Felman AH, Kirkpatrick JA.
    Am J Dis Child; 1970 Oct; 120(4):329-31. PubMed ID: 5493830
    [No Abstract] [Full Text] [Related]

  • 14. Langer type of mesomelic dwarfism as the possible homozygous expression of dyschondrosteosis.
    Fryns JP, Van Den Berghe H.
    Hum Genet; 1979 Jan 19; 46(1):21-7. PubMed ID: 429003
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Growth hormone treatment in Léri-Weill syndrome.
    Thuestad IJ, Ivarsson SA, Nilsson KO, Wattsgård C.
    J Pediatr Endocrinol Metab; 1996 Jan 19; 9(2):201-4. PubMed ID: 8887145
    [Abstract] [Full Text] [Related]

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

  • 18. Dyschondrostéose (Leri-Weill syndrome): congenital short forearms, Madelung-type wrist deformities, and moderate dwarfism.
    Berdon WE, Grossman H, Baker DH.
    Radiology; 1965 Oct 19; 85(4):677-81. PubMed ID: 5837961
    [No Abstract] [Full Text] [Related]

  • 19. [Dyschondrosteosis. Case report].
    Buffoni L, Pelizza A.
    Minerva Pediatr; 1967 Apr 07; 19(14):679-82. PubMed ID: 5613686
    [No Abstract] [Full Text] [Related]

  • 20. MESOMELIC DWARFISM (DYSCHONDROST'EOSE OF LERI AND WEILL).
    PINALS D, HEIMANN WG.
    JAMA; 1965 Sep 20; 193():1056-8. PubMed ID: 14340691
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.