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 *

389 related articles for article (PubMed ID: 474720)

  • 21. Molecular-pathogenetic classification of genetic disorders of the skeleton.
    Superti-Furga A; Bonafé L; Rimoin DL
    Am J Med Genet; 2001; 106(4):282-93. PubMed ID: 11891680
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Skeletal dysplasias and the growth plate.
    Alman BA
    Clin Genet; 2008 Jan; 73(1):24-30. PubMed ID: 18070126
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): a neonatally lethal short-limbed skeletal displasia.
    Sillence DO; Lachman RS; Jenkins T; Riccardi VM; Rimoin DL
    Am J Med Genet; 1982 Sep; 13(1):7-14. PubMed ID: 6753583
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Infantile thoracic dystrophy.
    Say B; Balci S; Tunçbilek E; Pirnar T
    Turk J Pediatr; 1969 Jul; 11(3):120-6. PubMed ID: 5392658
    [No Abstract]   [Full Text] [Related]  

  • 25. Tissue and cell studies of the growth plate in the chondrodysplasias.
    Horton WA; Campbell D; Machado MA; Aulthouse AL; Ahmed S; Ellard JT
    Am J Med Genet; 1989 Sep; 34(1):91-5. PubMed ID: 2816990
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Chondro-osseous morphology and biochemistry in the skeletal dysplasias.
    Rimoin DL; Sillence DO
    Birth Defects Orig Artic Ser; 1981; 17(1):249-65. PubMed ID: 7284584
    [No Abstract]   [Full Text] [Related]  

  • 27. [Diagnosis and nosological classification of micromelic nanism in the newborn infant].
    Marrone G; Cappello A
    Pediatria (Napoli); 1978 Mar; 86(1):155-67. PubMed ID: 98751
    [No Abstract]   [Full Text] [Related]  

  • 28. The role of mesenchyme-like tissue in the pathogenesis of thanatophoric dysplasia.
    Ornoy A; Adomian GE; Eteson DJ; Burgeson RE; Rimoin DL
    Am J Med Genet; 1985 Aug; 21(4):613-30. PubMed ID: 4025393
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The mouse skeletal mutants: models for the human skeletal dysplasias.
    Eteson DJ; Sillence DO; Lachman RS; Rimoin DL
    Prog Clin Biol Res; 1985; 187():141-51. PubMed ID: 4059229
    [No Abstract]   [Full Text] [Related]  

  • 30. Diastropic dwarfism: a histochemical and ultrastructural study of the endochondral growth plate.
    Horton WA; Rimoin DL; Hollister DW; Silberberg R
    Pediatr Res; 1979 Aug; 13(8):904-9. PubMed ID: 90360
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Oral manifestations in Ellis-van Creveld syndrome: report of five cases.
    Cahuana A; Palma C; Gonzáles W; Geán E
    Pediatr Dent; 2004; 26(3):277-82. PubMed ID: 15185812
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The genetics of short stature.
    Scott CI
    Prog Med Genet; 1972; 8():243-99. PubMed ID: 4259833
    [No Abstract]   [Full Text] [Related]  

  • 33. Spinal disorders associated with skeletal dysplasias and syndromes.
    Song D; Maher CO
    Neurosurg Clin N Am; 2007 Jul; 18(3):499-514. PubMed ID: 17678751
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Lethal osteosclerotic osteochondrodysplasia with platyspondyly, metaphyseal widening, and intracellular inclusions in sibs.
    Brodie SG; Lachman RS; Jewell AF; Winkler CL; Nolasco L; Wilcox WR
    Am J Med Genet; 1998 Dec; 80(4):423-8. PubMed ID: 9856576
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Inborn errors of cholesterol biosynthesis.
    Kelley RI
    Adv Pediatr; 2000; 47():1-53. PubMed ID: 10959439
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ellis-van Creveld syndrome. A report of previously undescribed anomalies in two siblings.
    Blackburn MG; Belliveau RE
    Am J Dis Child; 1971 Sep; 122(3):267-70. PubMed ID: 5568596
    [No Abstract]   [Full Text] [Related]  

  • 37. [Diagnosis of chondrodystrophic dwarfism in the newborn].
    Maroteaux P; Lamy M
    Arch Fr Pediatr; 1968 Mar; 25(3):241-62. PubMed ID: 4970273
    [No Abstract]   [Full Text] [Related]  

  • 38. Ultrastructure of cartilage in heritable disorders of connective tissue.
    Nogami H; Oohira A; Ozeki K; Oki T; Ogino T; Murachi S
    Clin Orthop Relat Res; 1979 Sep; (143):251-9. PubMed ID: 228885
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Abnormality of cartilage collagen in a patient with unclassified chondrodystrophy.
    Sussman MD; Kelly T; Rosenbaum KN; Balian G
    J Orthop Res; 1984; 2(4):339-45. PubMed ID: 6527159
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [The metabolic basis of generalized skeletal dysplasia (author's transl)].
    Spranger J
    Radiologe; 1976 Jul; 16(7):262-9. PubMed ID: 822473
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.