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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

205 related items for PubMed ID: 6661872

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  • 23. Scintigraphic findings in progressive diaphyseal dysplasia.
    Lundy MM, Billingsley JL, Redwine MD, Turnbull GL, Brown TJ.
    J Nucl Med; 1982 Apr; 23(4):324-5. PubMed ID: 6461731
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  • 27. Case report 202. Engelmann disease of bone (diaphyseal dysplasia) with bilateral shortened fibulae.
    Crisp AJ, Brenton DP, Shaw DG.
    Skeletal Radiol; 1982 Apr; 8(3):239-40. PubMed ID: 7112156
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  • 34. Immunological investigations in 2 families with progressive diaphyseal dysplasia.
    Pollack S, Naveh Y, Katz R.
    J Rheumatol; 1989 Sep; 16(9):1259-62. PubMed ID: 2810285
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  • 35. [Description of a case of Camurati-Engelmann syndrome in a newborn infant].
    Carbone R, Ponticelli A, Bernardo NS, Galasso GF.
    Pediatria (Napoli); 1983 Sep; 91(2-3):261-4. PubMed ID: 6664733
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  • 36. A generalized disorders of the connective tissues with progeria, choanal atresia, symphalangism, hypoplasia of dentine and craniodiaphyseal hypostosis.
    Lenz WD, Majewski F.
    Birth Defects Orig Artic Ser; 1974 Sep; 10(12):133-6. PubMed ID: 4376705
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  • 37. [Course of diaphyseal dysplasia. Camurati-Engelmann disease followed for 14 years].
    Marchal AL, Bretagne MC, Fourchy E, Olive D, Hoeffel JC.
    J Radiol; 1983 Dec; 64(12):675-9. PubMed ID: 6663565
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  • 40. Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13.
    Janssens K, Gershoni-Baruch R, Van Hul E, Brik R, Guañabens N, Migone N, Verbruggen LA, Ralston SH, Bonduelle M, Van Maldergem L, Vanhoenacker F, Van Hul W.
    J Med Genet; 2000 Apr; 37(4):245-9. PubMed ID: 10745041
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