BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 4541298)

  • 1. Osteopathia striata--Voorhoeve's disease. Review of the roentgen manifestations.
    Gehweiler JA; Bland WR; Carden TS; Daffner RH
    Am J Roentgenol Radium Ther Nucl Med; 1973 Jun; 118(2):450-5. PubMed ID: 4541298
    [No Abstract]   [Full Text] [Related]  

  • 2. Upington disease: a familial dyschondroplasia.
    Schweitzer G; Jones B; Timme A
    S Afr Med J; 1971 Sep; 45(36):994-1000. PubMed ID: 5316541
    [No Abstract]   [Full Text] [Related]  

  • 3. Osteopathia striata syndrome. Clinical, genetic and radiologic considerations.
    Bass HN; Weiner JR; Goldman A; Smith LE; Sparkes RS; Crandall BF
    Clin Pediatr (Phila); 1980 May; 19(5):369-73. PubMed ID: 6965904
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Frontometaphyseal dysplasia.
    Holt JF; Thompson GR; Arenberg IK
    Radiol Clin North Am; 1972 Aug; 10(2):225-43. PubMed ID: 5044403
    [No Abstract]   [Full Text] [Related]  

  • 5. Metachondromatosis.
    Lachman RS; Cohen A; Hollister D; Rimoin DL
    Birth Defects Orig Artic Ser; 1974; 10(9):171-8. PubMed ID: 4547387
    [No Abstract]   [Full Text] [Related]  

  • 6. [Osteopathia striata Voorhoeve (author's transl)].
    Kolár J
    Cesk Radiol; 1976 Jul; 30(4):268-73. PubMed ID: 1085657
    [No Abstract]   [Full Text] [Related]  

  • 7. Hereditary multiple exostoses. Anthropometric, roentgenographic, and clinical aspects.
    Shapiro F; Simon S; Glimcher MJ
    J Bone Joint Surg Am; 1979 Sep; 61(6A):815-24. PubMed ID: 225330
    [No Abstract]   [Full Text] [Related]  

  • 8. Multiple exostotic hypochondroplasia: syndrome of combined hypochondroplasia and multiple exostoses.
    Dominguez R; Young LW; Steele MW; Girdany BR
    Pediatr Radiol; 1984; 14(5):356-9. PubMed ID: 6332296
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial osteopathia striata with cranial condensation.
    Cortina H; Vallcanera A; Vidal J
    Pediatr Radiol; 1981; 11(2):87-90. PubMed ID: 7301452
    [No Abstract]   [Full Text] [Related]  

  • 10. [A combination of multiple cartilaginous exostoses and enchondromatosis of bone in a family].
    Tschernikoff Z; Ditscheva L
    Radiol Diagn (Berl); 1989; 30(1):53-6. PubMed ID: 2785276
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Metaphyseal dysplasia: a new autosomal dominant type in a large German kindred.
    Braun HS; Nürnberg P; Tinschert S
    Am J Med Genet; 2001 Jun; 101(1):74-7. PubMed ID: 11343343
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Micromelic dwarfism--humerus, femur, tibia type. Report of a case.
    Baxova A; Kozlowski K; Netriova I
    Pediatr Radiol; 1993; 23(6):446-9. PubMed ID: 8255648
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stüve-Wiedemann syndrome in a neonate.
    Sarafidis K; Piretzi K; Agakidou E; Kohlhase J; Zafeiriou D
    Pediatr Int; 2015 Apr; 57(2):302-4. PubMed ID: 25868946
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Roentgen rounds #89. Metachondromatosis.
    McAlister WH; Cacciarelli AA; Gilula LA
    Orthop Rev; 1987 Jul; 16(7):498-500. PubMed ID: 3502612
    [No Abstract]   [Full Text] [Related]  

  • 15. Multiple exostoses.
    Elliott DE
    Birth Defects Orig Artic Ser; 1974; 10(12):535-4. PubMed ID: 4549300
    [No Abstract]   [Full Text] [Related]  

  • 16. Progessive diaphyseal dysplasia. Review of the literature and report of seven cases in one family.
    Hundley JD; Wilson FC
    J Bone Joint Surg Am; 1973 Apr; 55(3):461-74. PubMed ID: 4703201
    [No Abstract]   [Full Text] [Related]  

  • 17. The radiographic patterns in dyschondrostosis.
    Hoeffel JC; Brauer B; Jimenez J; Hoeffel F
    Aust Paediatr J; 1972 Aug; 8(4):191-4. PubMed ID: 4539409
    [No Abstract]   [Full Text] [Related]  

  • 18. [Exostotic chondrodysplasia].
    Koval' GIu; Vasil'ev NA; Nesterovskaia VI; Sizov VA
    Klin Khir (1962); 1987; (12):5-8. PubMed ID: 3502160
    [No Abstract]   [Full Text] [Related]  

  • 19. Metachondromatosis. Report of four cases.
    Bassett GS; Cowell HR
    J Bone Joint Surg Am; 1985 Jun; 67(5):811-4. PubMed ID: 3873457
    [No Abstract]   [Full Text] [Related]  

  • 20. A novel nonsense mutation of the EXT1 gene in an Argentinian patient with multiple hereditary exostoses: a case report.
    Delgado MA; Sarrión P; Azar N; Zecchini L; Robledo HH; Segura F; Balcells S; Grinberg D; Dodelson de Kremer R; Asteggiano CG
    J Bone Joint Surg Am; 2012 Jun; 94(11):e76. PubMed ID: 22637216
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.