BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

94 related articles for article (PubMed ID: 4265809)

  • 1. [Pelvic bones in systemic diseases].
    Giesen H; Schmid F
    Fortschr Med; 1972 Sep; 90(27):980-4. PubMed ID: 4265809
    [No Abstract]   [Full Text] [Related]  

  • 2. [Pyknodysostosis. Nosological and pathogenetic classification].
    Sandomenico C; Del Vecchio E
    Radiol Med; 1967 Feb; 53(2):160-81. PubMed ID: 5188250
    [No Abstract]   [Full Text] [Related]  

  • 3. [Hereditary dysostoses].
    Swoboda W
    Fortschr Geb Rontgenstrahlen Nuklearmed Erganzungsbd; 1969; 78():40-98. PubMed ID: 4393888
    [No Abstract]   [Full Text] [Related]  

  • 4. [Embryonal osteochondropathies. Recent progress].
    Nigro N
    Minerva Pediatr; 1974 Jun; 26(20):1025-31. PubMed ID: 4210829
    [No Abstract]   [Full Text] [Related]  

  • 5. [Taxonomy of dysostoses].
    Schmid F
    Radiologe; 1967 Dec; 7(12):365-76. PubMed ID: 4968714
    [No Abstract]   [Full Text] [Related]  

  • 6. [Embryonal osteochondropathies with pelvic localization].
    Marchese GS; Pagani A
    Minerva Ortop; 1966 Sep; 17(9):514-8. PubMed ID: 5994465
    [No Abstract]   [Full Text] [Related]  

  • 7. [Growth retardation of skeletal origin: with special reference to osteochondrodysplasias].
    Bueno M; Bueno-Lozano M
    An Esp Pediatr; 1992 Jun; 36 Suppl 50():113-24. PubMed ID: 1416502
    [No Abstract]   [Full Text] [Related]  

  • 8. [Bone dysplasias and dystrophies. The viewpoint of the anatomo-pathologist].
    Chomette G; Auriol M
    Rev Stomatol Chir Maxillofac; 1987; 88(1):15-9. PubMed ID: 3551037
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [DOMINANT HEREDITARY SYNDROME, COMBINING CRANIO-FACIAL DYSOSTOSIS PECULIAR TYPE, GROWTH INSUFFICIENCY OF CHONDRODYSTROPHIC APPEARANCE, AND MASSIVE THICKENING OF OF THE CORTICES OF LONG BONES].
    STANESCO V; MAXIMILIAN C; POENARU S; FLOREA I; STANESCO R; IONESCO V; IOANITIU D
    Rev Fr Endocrinol Clin; 1963; 4():219-31. PubMed ID: 14049206
    [No Abstract]   [Full Text] [Related]  

  • 10. Genetic skeletal dysplasias in the Museum of Pathological Anatomy, Vienna.
    Beighton P; Sujansky E; Patzak B; Portele KA
    Am J Med Genet; 1993 Nov; 47(6):843-7. PubMed ID: 8279481
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic and Metabolic Conditions.
    Stankovits LM; Lopyan AH
    Pediatr Clin North Am; 2020 Feb; 67(1):23-43. PubMed ID: 31779835
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Picture of the month: pycnodysostosis.
    Gellis SS; Feingold M
    Am J Dis Child; 1967 Feb; 113(2):275-6. PubMed ID: 6019446
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic skeletal dysplasia in Thailand: the Siriraj experience.
    Wasant P; Waeteekul S; Rimoin DL; Lachman RS
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():59-67. PubMed ID: 8629144
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bone dysplasia in a child born to parents with osteogenesis imperfecta and pseudoachondroplasia.
    Kitoh H; Oki T; Arao K; Nogami H
    Am J Med Genet; 1994 Jul; 51(3):187-90. PubMed ID: 8074142
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Osteogenesis imperfecta and other heritable disorders of bone.
    Paterson CR
    Baillieres Clin Endocrinol Metab; 1997 Apr; 11(1):195-213. PubMed ID: 9222492
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Evaluation of bone mineral density in selected regions of the skeleton in children with osteogenesis imperfecta and hypophosphatemic rickets].
    Olszaniecka M; Lebiedowski M; Matusik H; RowiƄska E; Wieczorek E; Lorenc R
    Pol Tyg Lek; 1995 Nov; 50(44-47):32-4. PubMed ID: 8643422
    [No Abstract]   [Full Text] [Related]  

  • 17. Genetic disorders and bone affecting the craniofacial skeleton.
    Chacon GE; Ugalde CM; Jabero MF
    Oral Maxillofac Surg Clin North Am; 2007 Nov; 19(4):467-74, v. PubMed ID: 18088898
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Osteopathies of the newborn and the infant].
    De Toni G
    Munch Med Wochenschr; 1967 Apr; 109(15):815-23. PubMed ID: 4873396
    [No Abstract]   [Full Text] [Related]  

  • 19. Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?
    Moog U; Maroteaux P; Schrander-Stumpel CT; van Ooij A; Schrander JJ; Fryns JP
    J Med Genet; 1999 Nov; 36(11):856-8. PubMed ID: 10544232
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Pediatric radiology].
    Marchese GS
    Minerva Med; 1966 Feb; 57(16):692-5. PubMed ID: 5325683
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.