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Journal Abstract Search

80 related items for PubMed ID: 788811

  • 21. Hereditary metaphyseal dysostosis, Schmid type.
    Tuchinda C, Punnakanta L, Angsusingha K.
    J Med Assoc Thai; 1976 Apr; 59(4):180-2. PubMed ID: 1270943
    [No Abstract] [Full Text] [Related]

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  • 24. [Growth hormone treatment in secondary growth retardation].
    de Muinck Keizer-Schrama SM.
    Tijdschr Kindergeneeskd; 1988 May; 56 Suppl 1():33-9. PubMed ID: 3046057
    [No Abstract] [Full Text] [Related]

  • 25. Coffin-Lowry syndrome and premature tooth loss: a case report.
    Day P, Cole B, Welbury R.
    ASDC J Dent Child; 2000 May; 67(2):148-50. PubMed ID: 10826053
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  • 28. [Diastrophic dwarfism or "metaphyseal dysostosis"].
    Fauchier C, Régy JM, Combe P.
    Ann Pediatr (Paris); 1970 Dec 02; 17(12):876-81. PubMed ID: 4993571
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  • 30. Unique dwarfing, spondylometaphyseal skeletal dysplasia, with joint laxity and dentinogenesis imperfecta.
    Goldblatt J, Carman P, Sprague P.
    Am J Med Genet; 1991 May 01; 39(2):170-2. PubMed ID: 2063920
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  • 32. Craniofacial anthropometric analysis in several types of chondrodysplasia.
    Hunter AG.
    Am J Med Genet; 1996 Oct 02; 65(1):5-12. PubMed ID: 8914734
    [Abstract] [Full Text] [Related]

  • 33. Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect.
    Winterpacht A, Hilbert M, Schwarze U, Mundlos S, Spranger J, Zabel BU.
    Nat Genet; 1993 Apr 02; 3(4):323-6. PubMed ID: 7981752
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  • 35. [Adenosine deaminase and phosphodiesterase activity of the blood of children with various diseases].
    Socha J, Mrozikiewicz D, Schneider Z.
    Pediatr Pol; 1982 Apr 02; 57(7-8):497-502. PubMed ID: 6302629
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  • 37. [Adenosine deaminase deficiency].
    Taniguchi A, Kamatani N.
    Ryoikibetsu Shokogun Shirizu; 2001 Apr 02; (33):150-1. PubMed ID: 11462375
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  • 39. The spondylometaphyseal dysplasias. A tentative classification.
    Maroteaux P, Spranger J.
    Pediatr Radiol; 1991 Apr 02; 21(4):293-7. PubMed ID: 1870931
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