BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

104 related articles for article (PubMed ID: 7307190)

  • 21. [Fundamentals of clinical and roentgenologic skeletal diagnosis in childhood].
    Swoboda W
    Fortschr Geb Rontgenstrahlen Nuklearmed Erganzungsbd; 1969; 78():5-11. PubMed ID: 4393889
    [No Abstract]   [Full Text] [Related]  

  • 22. [Hypochondroplasia (author's transl)].
    Grepl J
    Cesk Radiol; 1980 Nov; 34(6):398-406. PubMed ID: 7249136
    [No Abstract]   [Full Text] [Related]  

  • 23. [Doughnut lesions of the cranial vault: an hereditary bone dysplasia].
    Aubé L; Vallières M; Lemay M
    Can Assoc Radiol J; 1988 Sep; 39(3):204-8. PubMed ID: 2971055
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Roentgen diagnosis of the growing skeleton].
    Swoboda W
    Fortschr Geb Rontgenstrahlen Nuklearmed Erganzungsbd; 1969; 78():11-40. PubMed ID: 4393878
    [No Abstract]   [Full Text] [Related]  

  • 25. Early skeletal hyperostoses secondary to 13-cis-retinoic acid.
    Pennes DR; Ellis CN; Madison KC; Voorhees JJ; Martel W
    AJR Am J Roentgenol; 1984 May; 142(5):979-83. PubMed ID: 6609585
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A "calcified suprasellar mass" in association with spondylometaphyseal dysplasia.
    Strand RD; Green B
    Ann Radiol (Paris); 1974; 17(4):369-74. PubMed ID: 4447311
    [No Abstract]   [Full Text] [Related]  

  • 27. [Hereditary generalized hyperostosis and enostosis].
    Tymchishin AO
    Vestn Rentgenol Radiol; 1977; (3):81-6. PubMed ID: 883125
    [No Abstract]   [Full Text] [Related]  

  • 28. Pyle's disease or craniometaphyseal dysplasia (tarda).
    Small PG; Wallis JJ
    Br J Radiol; 1970 Nov; 43(515):811-3. PubMed ID: 5475777
    [No Abstract]   [Full Text] [Related]  

  • 29. The radiological manifestations of metaphyseal dysplasia (Pyle disease).
    Heselson NG; Raad MS; Hamersma H; Cremin BJ; Beighton P
    Br J Radiol; 1979 Jun; 52(618):431-40. PubMed ID: 465917
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Familial metaphyseal dysplasia (Pyle's disease) versus craniometaphyseal dysplasia. Presentation of a case].
    Gambardella A; Ciccarelli R; Pepe A; Mosca A
    Radiol Med; 1990 Sep; 80(3):360-3. PubMed ID: 2236701
    [No Abstract]   [Full Text] [Related]  

  • 31. Craniometaphyseal dysplasia. A family with three documented cases.
    Carlson DH; Harris GB
    Radiology; 1972 Apr; 103(1):147-51. PubMed ID: 4335672
    [No Abstract]   [Full Text] [Related]  

  • 32. [Unusual case of hypertrophic polyostotic osteopathy].
    Trinchi E; Aldegheri R
    Clin Ortop; 1973; 24(4):256-67. PubMed ID: 4806191
    [No Abstract]   [Full Text] [Related]  

  • 33. 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]  

  • 34. Sclerosteosis in old age.
    Barnard AH; Hamersma H; Kretzmar JH; Beighton P
    S Afr Med J; 1980 Sep; 58(10):401-3. PubMed ID: 7404164
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Case of craniometaphyseal dysplasia considered to be typical in x-ray figures].
    Katsumata N; Tanabe M; Aono K; Morino Y; Watanabe S
    Rinsho Hoshasen; 1971 Aug; 16(8):637-42. PubMed ID: 5209368
    [No Abstract]   [Full Text] [Related]  

  • 36. Craniotubular bone disorders.
    Gorlin RJ
    Pediatr Radiol; 1994; 24(6):392-406. PubMed ID: 7700714
    [No Abstract]   [Full Text] [Related]  

  • 37. [Relationships between skeletal development and mental disorders].
    Silinkovà-Màlkovà E; Balcar V; Silink K; Kremenovà J; Blehovà B
    Cesk Radiol; 1973; 27(4):217-27. PubMed ID: 4726588
    [No Abstract]   [Full Text] [Related]  

  • 38. Primary protrusio acetabuli. Report of an affected family.
    Macdonald D
    J Bone Joint Surg Br; 1971 Feb; 53(1):30-6. PubMed ID: 5578763
    [No Abstract]   [Full Text] [Related]  

  • 39. [A case of osteopathia striata].
    Bernard C; Hoeffel JC; Merle M; Fourchy E
    Sem Hop; 1984 Feb; 60(8):573-6. PubMed ID: 6322343
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Skeletal dysplasia, occipital horns, diarrhea and obstructive uropathy- a new hereditary syndrome.
    Lazoff SG; Rybak JJ; Parker BR; Luzzatti L
    Birth Defects Orig Artic Ser; 1975; 11(5):71-4. PubMed ID: 1218238
    [No Abstract]   [Full Text] [Related]  

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