BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 8152878)

  • 21. [Familial craniometaphyseal dysplasia associated with mental retardation].
    Portnov VA; Marincheva GS; Gorbachevskaia NL
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1985; 85(3):404-9. PubMed ID: 3993302
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Metaphyseal and epiphyseal dysplasia with unusual facies and cataract.
    Kozlowski K; Rafinski T; Kucharska K
    Am J Dis Child; 1973 Apr; 125(4):553-6. PubMed ID: 4699894
    [No Abstract]   [Full Text] [Related]  

  • 23. Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs.
    Toledo SP; Saldanha PH; Lamego C; Mourão PA; Dietrich CP; Mattar E
    Am J Med Genet; 1979; 4(3):255-61. PubMed ID: 117710
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Wedge-shaped epiphyses of the knees in two siblings: a new recessive rare dysplasia?
    Bellini F; Chiumello G; Rimoldi R; Weber G
    Helv Paediatr Acta; 1984 Oct; 39(4):365-72. PubMed ID: 6543849
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The Dyggve-Melchior-Clausen syndrome in Indian siblings.
    Winship WS; Rubin DL
    Clin Genet; 1992 Nov; 42(5):240-5. PubMed ID: 1486701
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Pelvic dysplasia associated with arthrogrypotic changes in the lower extremities. A new syndrome.
    Ray S; Peterson PD; Scott CI
    Clin Orthop Relat Res; 1986 Jun; (207):99-102. PubMed ID: 3720110
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Asphyxiating thoracic dysplasia. Clinical, radiological, and pathological information on 10 patients.
    Oberklaid F; Danks DM; Mayne V; Campbell P
    Arch Dis Child; 1977 Oct; 52(10):758-65. PubMed ID: 931421
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Combination of rare anomalies of the cervical spine and peripheral skeleton].
    Loreck D; Buttgereit F; Burmester GR
    Aktuelle Radiol; 1995 Jul; 5(4):235-7. PubMed ID: 7548249
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Deafness, onycho-osteodystrophy, mental retardation (DOOR) syndrome.
    Nevin NC; Thomas PS; Calvert J; Reid MM
    Am J Med Genet; 1982 Nov; 13(3):325-32. PubMed ID: 7180877
    [No Abstract]   [Full Text] [Related]  

  • 30. Metaphyseal dysostosis, Jansen type.
    Arroyo-Scotoliff H
    J Bone Joint Surg Am; 1973 Apr; 55(3):623-9. PubMed ID: 4634045
    [No Abstract]   [Full Text] [Related]  

  • 31. Rapidly progressive scoliosis in multiple epiphyseal dysplasia. A case report.
    Herring JA
    J Bone Joint Surg Am; 1976 Jul; 58(5):703-4. PubMed ID: 932068
    [No Abstract]   [Full Text] [Related]  

  • 32. [Fronto-metaphyseal dysplasia].
    Sauvegrain J; Lombard M; Garel L; Truscelli D
    Ann Radiol (Paris); 1975 Mar; 18(2):155-62. PubMed ID: 1094899
    [No Abstract]   [Full Text] [Related]  

  • 33. A bone dysplasia with deafness.
    Insley J; Astley R
    Br J Radiol; 1974 May; 47(557):244-51. PubMed ID: 4830146
    [No Abstract]   [Full Text] [Related]  

  • 34. [Dyggve-Melchior-Clausen dysplasia (apropos of a case)].
    Sbihi A; Benharbit R; Lahrichi A; Lahrech MT
    Maghrib Tibbi; 1980 Dec; 2(4):367-74. PubMed ID: 7345231
    [No Abstract]   [Full Text] [Related]  

  • 35. An unusual bone dysplasia: parastremmatic dwarfism.
    Langer LO; Petersen D; Spranger J
    Am J Roentgenol Radium Ther Nucl Med; 1970 Nov; 110(3):550-60. PubMed ID: 4992387
    [No Abstract]   [Full Text] [Related]  

  • 36. Variability of spondylo-metaphyseal dysplasia, common type.
    Kozlowski K; Cremin B; Beighton P
    Radiol Diagn (Berl); 1980; 21(5):682-6. PubMed ID: 7244191
    [No Abstract]   [Full Text] [Related]  

  • 37. Chondrodystrophy-mucopolysaccharidosis disparity.
    Milicic M; Peterson HA
    Clin Orthop Relat Res; 1971 Oct; 80():92-104. PubMed ID: 4257268
    [No Abstract]   [Full Text] [Related]  

  • 38. Skeletal dysplasia, intracerebral calcifications, optic atrophy, hearing impairment, and mental retardation: nosology of dysosteosclerosis.
    Chitayat D; Silver K; Azouz EM
    Am J Med Genet; 1992 Jun; 43(3):517-23. PubMed ID: 1605243
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A Croatian case of the Schinzel-Giedion syndrome.
    Culić V; Resic B; Oorthuys JW; Overweg-Plandsoen WC; Hennekam RC
    Genet Couns; 1996; 7(1):21-5. PubMed ID: 8652084
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Sotos' syndrome (cerebral gigantism) with peripheral dysostosis.
    Evans PR
    Arch Dis Child; 1971 Apr; 46(246):199-202. PubMed ID: 5089596
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.