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Journal Abstract Search

299 related items for PubMed ID: 8213919

  • 21. Clinical, radiographic, pathologic, and genetic features of osteochondrodysplasia in Scottish deerhounds.
    Breur GJ, Zerbe CA, Slocombe RF, Padgett GA, Braden TD.
    J Am Vet Med Assoc; 1989 Sep 01; 195(5):606-12. PubMed ID: 2777707
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  • 22. A new case of Greenberg dysplasia and literature review suggest that Greenberg dysplasia, dappled diaphyseal dysplasia, and Astley-Kendall dysplasia are allelic disorders.
    Gregersen PA, McKay V, Walsh M, Brown E, McGillivray G, Savarirayan R.
    Mol Genet Genomic Med; 2020 Jun 01; 8(6):e1173. PubMed ID: 32304187
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  • 23. Acromicric dysplasia.
    Maroteaux P, Stanescu R, Stanescu V, Rappaport R.
    Am J Med Genet; 1986 Jul 01; 24(3):447-59. PubMed ID: 3728563
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  • 24. [Lethal osteo-chondro-dysplasia: feto-pathological study of 32 cases].
    Lahmar-Boufaroua A, Yacoubi MT, Hmisssa S, Selmi M, Korbi S.
    Tunis Med; 2009 Feb 01; 87(2):127-32. PubMed ID: 19522446
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  • 26. Ultrastructural abnormalities in bone and calcifying cartilage in two siblings with a newly described recessive lethal chondrodysplasia.
    Gruber HE, Greenberg CR, Lachman RS, Rimoin DL.
    Ultrastruct Pathol; 1990 Feb 01; 14(4):343-55. PubMed ID: 2382311
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  • 27. Further delineation of spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type, with emphasis on diagnostic features.
    Langer LO, Wolfson BJ, Scott CI, Reid CS, Schidlow DV, Millar EA, Borns PF, Lubicky JP, Carpenter BL.
    Am J Med Genet; 1993 Feb 15; 45(4):488-500. PubMed ID: 8465857
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  • 29. Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome presenting with a large nephrogenic cyst, severe oligohydramnios and hydrops fetalis: a case report and review of the literature.
    Chuangsuwanich T, Sunsaneevithayakul P, Muangsomboon K, Limwongse C.
    Prenat Diagn; 2005 Mar 15; 25(3):210-5. PubMed ID: 15791665
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  • 31. Distinct, autosomal recessive form of spondyloepimetaphyseal dysplasia segregating in an inbred Pakistani kindred.
    Ahmad M, Faiyaz Ul Haque M, Ahmad W, Abbas H, Haque S, Krakow D, Rimoin DL, Lachman RS, Cohn DH.
    Am J Med Genet; 1998 Aug 06; 78(5):468-73. PubMed ID: 9714015
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  • 32. Achondrogenesis type II with polydactyly.
    Rittler M, Orioli IM.
    Am J Med Genet; 1995 Nov 06; 59(2):157-60. PubMed ID: 8588578
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  • 36. [The difficulty of prenatal diagnosis of Kniest's disease. Apropos of a case simulating congenital spondylo-epiphyseal dysplasia].
    Kerleroux J, Roux MS, Cottin X.
    J Gynecol Obstet Biol Reprod (Paris); 1994 Nov 06; 23(1):69-74. PubMed ID: 8157894
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  • 37. Antenatal Phenotype of Desbuquois Dysplasia.
    Biji IK, Mahay SB, Saxena R, Verma I, Kumar B, Puri RD.
    Indian J Pediatr; 2023 Jan 06; 90(1):83-86. PubMed ID: 36331722
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  • 39. Skeletal ciliopathies: a pattern recognition approach.
    Handa A, Voss U, Hammarsjö A, Grigelioniene G, Nishimura G.
    Jpn J Radiol; 2020 Mar 06; 38(3):193-206. PubMed ID: 31965514
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  • 40. Lethal short-limbed chondrodysplasia in early infancy.
    Yang SS, Heidelberger KP, Brough AJ, Corbett DP, Bernstein J.
    Perspect Pediatr Pathol; 1976 Mar 06; 3():1-40. PubMed ID: 972830
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