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Journal Abstract Search

140 related items for PubMed ID: 8577560

  • 1. Perlman syndrome: report of a case with additional radiographic findings.
    Herman TE, McAlister WH.
    Pediatr Radiol; 1995 Nov; 25 Suppl 1():S70-2. PubMed ID: 8577560
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  • 3. Rare clinical entity Perlman syndrome: is cholestasis a new finding?
    Demirel G, Oguz SS, Celik IH, Uras N, Erdeve O, Dilmen U.
    Congenit Anom (Kyoto); 2011 Mar; 51(1):43-5. PubMed ID: 20726997
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  • 5. The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies.
    Neri G, Martini-Neri ME, Katz BE, Opitz JM.
    Am J Med Genet; 1984 Sep; 19(1):195-207. PubMed ID: 6093533
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  • 6. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome.
    al-Gazali LI, Bakir M, Sadaghatian MR, Nath R, Haas D.
    Clin Dysmorphol; 1999 Apr; 8(2):87-92. PubMed ID: 10319196
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  • 8. The Perlman familial nephroblastomatosis syndrome.
    Greenberg F, Stein F, Gresik MV, Finegold MJ, Carpenter RJ, Riccardi VM, Beaudet AL.
    Am J Med Genet; 1986 May; 24(1):101-10. PubMed ID: 3010722
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  • 9. Perlman syndrome: report, prenatal findings and review.
    Alessandri JL, Cuillier F, Ramful D, Ernould S, Robin S, de Napoli-Cocci S, Rivière JP, Rossignol S.
    Am J Med Genet A; 2008 Oct 01; 146A(19):2532-7. PubMed ID: 18780370
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  • 10. A case of Perlman syndrome presenting with hemorrhagic hemangioma.
    Pirgon O, Atabek ME, Akin F, Sert A.
    J Pediatr Hematol Oncol; 2006 Aug 01; 28(8):531-3. PubMed ID: 16912594
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  • 11. [The cerebro-oculo-facio-skeletal syndrome].
    Piussan C, Cuvelier B, Lenaerts C, Le Mareschal B, Réguet C, Risbourg B.
    Arch Fr Pediatr; 1979 Apr 01; 36(4):379-86. PubMed ID: 496530
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  • 14. Schinzel-Giedion syndrome: autopsy report and additional clinical manifestations.
    Rodríguez JI, Jiménez-Heffernan JA, Leal J.
    Am J Med Genet; 1994 Dec 01; 53(4):374-7. PubMed ID: 7864048
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  • 15. [Osteoglophonic skeletal dysplasia--a variant of generalized fibrous dysplasia? Case report and review of the literature].
    Stöss H, Sieber E, Tietze HU.
    Pathologe; 1991 May 01; 12(3):161-6. PubMed ID: 1876584
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  • 20. Possible new autosomal recessive syndrome with unusual renal histopathological changes.
    Allanson JE, Pantzar JT, MacLeod PM.
    Am J Med Genet; 1983 Sep 01; 16(1):57-60. PubMed ID: 6638071
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