These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 13349278)

  • 41. [Polyepiphyseal dystrophy].
    SERRE H; PERRIER M
    Montp Med; 1959; 56():18-23. PubMed ID: 14445117
    [No Abstract]   [Full Text] [Related]  

  • 42. [Ollier's disease. Pathogenetic problems and therapeutic possibilities].
    BETHGE JF
    Dtsch Med Wochenschr; 1962 Mar; 87():535-41. PubMed ID: 13868609
    [No Abstract]   [Full Text] [Related]  

  • 43. [Apropos of an extremely rare disorder: observation of a case of hereditary osteo-onychodysplasia (Turner's syndrome)].
    MARC R; LE GUIFFANT M; LE TREUT A; MORIN G
    J Med Bord; 1959 Dec; 136():1351-7. PubMed ID: 14420841
    [No Abstract]   [Full Text] [Related]  

  • 44. [Congenital abnormalities and anomalies. 3. Dyschondrosteosis (Leri-Weil syndrome) with report on an additional case)].
    KIRCHMAIR H
    Med Monatsschr; 1962 Mar; 16():174-5. PubMed ID: 14456251
    [No Abstract]   [Full Text] [Related]  

  • 45. [Fetal hyperplastic chondrodystrophy with meta- and hyperplasia].
    DAVID H
    Zentralbl Allg Pathol; 1958 Dec; 98(9-11):550-5. PubMed ID: 13625966
    [No Abstract]   [Full Text] [Related]  

  • 46. [About a polyepiphyseal dystrophy observed from at the infantile medical clinic of Algiers].
    GILLOT F; SENDRA L; GUENOUN M
    Pediatrie; 1956; 11(4):470-2. PubMed ID: 13349379
    [No Abstract]   [Full Text] [Related]  

  • 47. [Chondrodystrophia calcificans congenita (stippled epiphyses)].
    UGLAND OM
    Nord Med; 1958 Jan; 59(5):194-5. PubMed ID: 13517610
    [No Abstract]   [Full Text] [Related]  

  • 48. Chondrodystrophia congenita punctata (Conradi's disease). Review of literature and report of case with unusual features.
    ALLANSMITH M; SENZ E
    Am J Dis Child; 1960 Jul; 100():109-16. PubMed ID: 13792702
    [No Abstract]   [Full Text] [Related]  

  • 49. Chondrodysplasia epiphysalis multiplex with diabetes mellitus and mental retardation.
    NORMAN AP
    Proc R Soc Med; 1961 Apr; 54(4):333-5. PubMed ID: 13729567
    [No Abstract]   [Full Text] [Related]  

  • 50. [Late spondyloepiphyseal dysplasia; clinical and radiological description].
    MAROTEAUX P; LAMY M; BERNARD J
    Presse Med (1893); 1957 Jun; 65(51):1205-8. PubMed ID: 13453331
    [No Abstract]   [Full Text] [Related]  

  • 51. Multiple stage leg-lengthening: report of a case of chondrodysplasia with a surgical increase of ten inches.
    URIST MR
    Proc R Soc Med; 1961 Oct; 54(10):864-8. PubMed ID: 13923922
    [No Abstract]   [Full Text] [Related]  

  • 52. [Heredity of chondrodysplasia].
    GREBE H
    Zentralbl Gynakol; 1951; 73(19):1552-8. PubMed ID: 14893943
    [No Abstract]   [Full Text] [Related]  

  • 53. [Chondrodysplasia (-dystrophia) fetalis hyperplastica in microradiographic studies].
    THURNER J; MIGNANI G; HUSSL B
    Virchows Arch Pathol Anat Physiol Klin Med; 1959; 332():407-19. PubMed ID: 13838274
    [No Abstract]   [Full Text] [Related]  

  • 54. [Pfaundler-Hurler's osteochondrodystrophy and its relations with metaepiphyseal mesenchymodystrophy of growth].
    PISANI G; CONTI T
    Chir Organi Mov; 1957; 44(1):1-17. PubMed ID: 13437387
    [No Abstract]   [Full Text] [Related]  

  • 55. [For the differential diagnosis of chondrodystrophy].
    FISCHER G
    Kinderarztl Prax; 1958 May; 26(5):204-8. PubMed ID: 13550480
    [No Abstract]   [Full Text] [Related]  

  • 56. Localized epiphyseal dysplasia in offspring of manganese-deficient rats.
    HURLEY LS; ASLING CW
    Anat Rec; 1963 Jan; 145():25-37. PubMed ID: 13955844
    [No Abstract]   [Full Text] [Related]  

  • 57. Punctate epiphyseal dysplasia, another cause of leg length inequality.
    WENZL JE; IVINS JC; STICKLER GB
    J Pediatr; 1961 Sep; 59():390-3. PubMed ID: 13784405
    [No Abstract]   [Full Text] [Related]  

  • 58. Comments on the rate of mutation to chondrodystrophy in man.
    SLATIS HM
    Am J Hum Genet; 1955 Mar; 7(1):76-9. PubMed ID: 14361397
    [No Abstract]   [Full Text] [Related]  

  • 59. [Description of a case of congenital luxation of the radius head in combination with signs of multiple cartilage exostoses and with symptoms of dyschondroplasia].
    van MEEL P
    Z Orthop Ihre Grenzgeb; 1962 Feb; 95():351-7. PubMed ID: 14472048
    [No Abstract]   [Full Text] [Related]  

  • 60. [Contribution to endochondral dysostosis].
    CRASSELT C
    Z Orthop Ihre Grenzgeb; 1962 Jun; 96():28-42. PubMed ID: 13882039
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.