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Journal Abstract Search

232 related items for PubMed ID: 4080742

  • 21. The type II collagenopathies: a spectrum of chondrodysplasias.
    Spranger J, Winterpacht A, Zabel B.
    Eur J Pediatr; 1994 Feb; 153(2):56-65. PubMed ID: 8157027
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  • 22. Craniofacial defects in the human skeletal dysplasias.
    Eteson DJ, Stewart RE.
    Birth Defects Orig Artic Ser; 1984 Feb; 20(3):19-45. PubMed ID: 6391575
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  • 23. Evaluation of newborns with skeletal dysplasias.
    Macpherson RI, Pai GS.
    Indian J Pediatr; 2000 Dec; 67(12):907-13. PubMed ID: 11262990
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  • 27. [Genetic basis for skeletal disease. Radiological approach for genetic skeletal disorders].
    Nishimura G.
    Clin Calcium; 2010 Aug; 20(8):1175-81. PubMed ID: 20675927
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  • 29. Dwarfism in the newborn: the nomenclature, radiological features and genetic significance.
    Cremin BJ, Beighton P.
    Br J Radiol; 1974 Feb; 47(554):77-93. PubMed ID: 4206212
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  • 33. Advances in bone dysplasias.
    Spranger J.
    Prog Clin Biol Res; 1982 Feb; 103 Pt B():323-32. PubMed ID: 7163228
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  • 36. ["Facing"--a preliminary parameter in diagnosis of fetal skeletal abnormalities].
    Krause M, Feige A.
    Geburtshilfe Frauenheilkd; 1993 Mar; 53(3):186-7. PubMed ID: 8467986
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  • 38. The genetic basis of the osteochondrodysplasias.
    Baitner AC, Maurer SG, Gruen MB, Di Cesare PE.
    J Pediatr Orthop; 2000 Mar; 20(5):594-605. PubMed ID: 11008738
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  • 39. Thanatophoric dysplasia in identical twins.
    Young ID, Patel I, Lamont AC.
    J Med Genet; 1989 Apr; 26(4):276-9. PubMed ID: 2716037
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