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Journal Abstract Search

185 related items for PubMed ID: 6212507

  • 1. [Mesomelic dwarfism of the Langer type as a homozygous form of dyschondrosteosis (author's transl)].
    Kemperdick H, Majewski F.
    Rofo; 1982 May; 136(5):583-7. PubMed ID: 6212507
    [No Abstract] [Full Text] [Related]

  • 2. Mesomelic dwarfism as the homozygous expression of dyschondrosteosis.
    Espiritu C, Chen H, Woolley PV.
    Am J Dis Child; 1975 Mar; 129(3):375-7. PubMed ID: 1121969
    [No Abstract] [Full Text] [Related]

  • 3. [Mesomelic dwarfism (author's transl)].
    Kemperdick H, Janssen F, Lenz W.
    Rofo; 1975 Nov; 123(5):450-4. PubMed ID: 128504
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  • 4. Dyschondrosteosis (mesomelic dwarfism)--a family study.
    Carter AR, Currey HL.
    Br J Radiol; 1974 Oct; 47(562):634-40. PubMed ID: 4433973
    [No Abstract] [Full Text] [Related]

  • 5. Micromelic dwarfism--humerus, femur, tibia type. Report of a case.
    Baxova A, Kozlowski K, Netriova I.
    Pediatr Radiol; 1993 Oct; 23(6):446-9. PubMed ID: 8255648
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  • 12. [Study of the classification of chondrodysplasias with mesomelic predominance].
    Maroteaux P, Spranger J.
    Arch Fr Pediatr; 1977 Dec; 34(10):945-58. PubMed ID: 610660
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  • 13. Mesomelic dwarfism of the hypoplastic ulna, fibula, mandible type.
    Langer LO.
    Radiology; 1967 Oct; 89(4):654-60. PubMed ID: 6059604
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  • 17. [Familial mesomelial dwarfism (Nievergelt syndrome)].
    Hess OM, Goebel NH, Streuli R.
    Schweiz Med Wochenschr; 1978 Aug 05; 108(31):1202-6. PubMed ID: 675214
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  • 18. Microdeletions on 6p22.3 are associated with mesomelic dysplasia Savarirayan type.
    Flöttmann R, Wagner J, Kobus K, Curry CJ, Savarirayan R, Nishimura G, Yasui N, Spranger J, Van Esch H, Lyons MJ, DuPont BR, Dwivedi A, Klopocki E, Horn D, Mundlos S, Spielmann M.
    J Med Genet; 2015 Jul 05; 52(7):476-83. PubMed ID: 26032025
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  • 19. [Clinical variations in Léri-Weill dyschondrosteosis].
    Duro EA, Prado GS.
    An Esp Pediatr; 1990 Nov 05; 33(5):461-3. PubMed ID: 2096761
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  • 20. [Mesomelic dwarfism Langer type associated to mixed gonadal dysgenesis, whit cariotipe 46,XY/45 X (author's transl)].
    Ruíz Gómez MJ, Martínez González M, Machín Jiménez AR, Fernández Villahoz AL.
    An Esp Pediatr; 1979 Dec 05; 12(12):897-904. PubMed ID: 533057
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