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Journal Abstract Search

204 related items for PubMed ID: 10781242

  • 1. Jansen's metaphyseal chondrodysplasia.
    Sood A, Sama D, Sharma R, Rastogi S.
    Indian Pediatr; 2000 Apr; 37(4):435-40. PubMed ID: 10781242
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  • 5. [Leri-Weill syndrome].
    Ogata T, Fukami M.
    Nihon Rinsho; 2006 Sep 28; Suppl 3():427-32. PubMed ID: 17022580
    [No Abstract] [Full Text] [Related]

  • 6. Murk Jansen's metaphyseal chondrodysplasia with long-term followup.
    Silverthorn KG, Houston CS, Duncan BP.
    Pediatr Radiol; 1987 Sep 28; 17(2):119-23. PubMed ID: 3562109
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  • 7. Constitutively activated receptors for parathyroid hormone and parathyroid hormone-related peptide in Jansen's metaphyseal chondrodysplasia.
    Schipani E, Langman CB, Parfitt AM, Jensen GS, Kikuchi S, Kooh SW, Cole WG, Jüppner H.
    N Engl J Med; 1996 Sep 05; 335(10):708-14. PubMed ID: 8703170
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  • 8. Osteochondrodystrophies with marked platyspondyly and distinctive peripheral anomalies.
    Kozlowski K, Bieganski T, Gardner J, Beighton P.
    Pediatr Radiol; 1999 Jan 05; 29(1):1-5. PubMed ID: 9880606
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  • 9. Chondrodysplasia punctata in a nine-year-old girl presenting as "unclassified multiple malformation syndrome".
    Kozlowski K.
    Pediatr Radiol; 1980 Jul 05; 9(4):236-8. PubMed ID: 7402749
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  • 10. [Metaphyseal chondrodysplasia (metaphyseal dysostosis)--a new type?].
    Wiedemann HR, Spranger J.
    Z Kinderheilkd; 1970 Jul 05; 108(2):171-86. PubMed ID: 4252978
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  • 11. Hypophosphatemia with elevations in serum fibroblast growth factor 23 in a child with Jansen's metaphyseal chondrodysplasia.
    Brown WW, Jüppner H, Langman CB, Price H, Farrow EG, White KE, McCormick KL.
    J Clin Endocrinol Metab; 2009 Jan 05; 94(1):17-20. PubMed ID: 18854401
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  • 14. Metaphyseal chondrodysplasia, McKusick type (cartilage hair hypoplasia).
    Sensenbrenner JA.
    Birth Defects Orig Artic Ser; 1974 Jan 05; 10(12):422-4. PubMed ID: 4549299
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  • 15. Metacarpophalangeal pattern profile analysis in diastrophic dysplasia.
    Butler MG, Gale DD, Meaney FJ.
    Am J Med Genet; 1987 Nov 05; 28(3):685-9. PubMed ID: 3425635
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  • 17. Multiple metaphyseal lesions in a child with a syndrome of progressive muscle cramps, alopecia and stunted growth (Satoyoshi disease).
    Matsuo N, Fujioka M, Tsuchiya Y, Cho H, Nagai T, Kumagai M.
    Radiat Med; 1983 Nov 05; 1(3):205-7. PubMed ID: 6680196
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  • 18. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL) in three neonates.
    Christianson AL, Beighton P.
    Genet Couns; 1996 Nov 05; 7(3):219-25. PubMed ID: 8897044
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  • 19. Léri dyschondrosteosis.
    Sensenbrenner JA.
    Birth Defects Orig Artic Ser; 1974 Nov 05; 10(12):448-52. PubMed ID: 4461079
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  • 20. Atypical skeletal changes in otopalatodigital syndrome type II: phenotypic overlap among otopalatodigital syndrome type II, boomerang dysplasia, atelosteogenesis type I and type III, and lethal male phenotype of Melnick-Needles syndrome.
    Nishimura G, Horiuchi T, Kim OH, Sasamoto Y.
    Am J Med Genet; 1997 Dec 12; 73(2):132-8. PubMed ID: 9409862
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