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Journal Abstract Search

90 related items for PubMed ID: 6650565

  • 1. Brachyolmia, recessive type (Hobaek): a clinical, radiographic, and histochemical study.
    Horton WA, Langer LO, Collins DL, Dwyer C.
    Am J Med Genet; 1983 Oct; 16(2):201-11. PubMed ID: 6650565
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  • 4. Dyssegmental dysplasias: clinical, radiographic, and morphologic evidence of heterogeneity.
    Aleck KA, Grix A, Clericuzio C, Kaplan P, Adomian GE, Lachman R, Rimoin DL.
    Am J Med Genet; 1987 Jun; 27(2):295-312. PubMed ID: 3605216
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  • 5. Short trunk stature, brachydactyly, and platyspondyly in three sibs: a new form of brachyolmia or a new skeletal dysplasia?
    Tüysüz B, Ungür S.
    Am J Med Genet A; 2003 Jun 15; 119A(3):375-80. PubMed ID: 12784309
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  • 6. Two sibs with brachyolmia type Hobaek: five year follow-up through puberty.
    Hoo JJ, Oliphant M.
    Am J Med Genet A; 2003 Jan 01; 116A(1):80-4. PubMed ID: 12476457
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  • 7. Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literature.
    Klinge L, Schaper J, Wieczorek D, Voit T.
    Neuropediatrics; 2002 Dec 01; 33(6):309-13. PubMed ID: 12571786
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  • 9. Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand type: a congenital familial skeletal dysplasia with distinctive features and histopathology.
    Borochowitz Z, Langer LO, Gruber HE, Lachman R, Katznelson MB, Rimoin DL.
    Am J Med Genet; 1993 Feb 01; 45(3):320-6. PubMed ID: 8434618
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  • 10. A further case of opsismodysplasia with hydrocephalus.
    Ramos FJ, González JP, Cortabarria C, Domenech E, Pérez-González J, Bueno M.
    Eur J Med Genet; 2006 Feb 01; 49(1):93-100. PubMed ID: 16473316
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  • 11. Static compressive loading reduces the mRNA expression of type II and X collagen in rat growth-plate chondrocytes during postnatal growth.
    Villemure I, Chung MA, Seck CS, Kimm MH, Matyas JR, Duncan NA.
    Connect Tissue Res; 2005 Feb 01; 46(4-5):211-9. PubMed ID: 16546824
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  • 13. Monozygotic twins discordant for spondylocostal dysostosis.
    Van Thienen MN, Van der Auwera BJ.
    Am J Med Genet; 1994 Oct 01; 52(4):483-6. PubMed ID: 7747763
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  • 15. Additional case of opsismodysplasia supporting autosomal recessive inheritance.
    Beemer FA, Kozlowski KS.
    Am J Med Genet; 1994 Feb 01; 49(3):344-7. PubMed ID: 8209898
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  • 18. Congenital lethal metaphyseal chondrodysplasia: a newly recognized complex autosomal recessive disorder.
    Sedaghatian MR.
    Am J Med Genet; 1980 Feb 01; 6(4):269-74. PubMed ID: 7211944
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  • 19. Biochemical abnormalities in connective tissue of osteodysplasty of Melnick-Needles and dyssegmental dwarfism.
    Svejcar J.
    Clin Genet; 1983 May 01; 23(5):369-75. PubMed ID: 6851229
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