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Journal Abstract Search

91 related items for PubMed ID: 9211556

  • 21.
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  • 22. The Meckel syndrome in the Hutterites.
    Schurig V, Bowen P, Harley F, Schiff D.
    Am J Med Genet; 1980; 5(4):373-81. PubMed ID: 7395917
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  • 23. Survival and spectrum of anomalies in the Meckel syndrome.
    Lowry RB, Hill RH, Tischler B.
    Am J Med Genet; 1983 Mar; 14(3):417-21. PubMed ID: 6859092
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  • 29. [Meckel-Gruber syndrome].
    Kondo I.
    Ryoikibetsu Shokogun Shirizu; 2000 Mar; (30 Pt 5):18-20. PubMed ID: 11057128
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  • 30. Skeletal malformations in fetuses with Meckel syndrome.
    Kjaer KW, Fischer Hansen B, Keeling JW, Kjaer I.
    Am J Med Genet; 1999 Jun 11; 84(5):469-75. PubMed ID: 10360401
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  • 31. An unclassifiable short rib-polydactyly syndrome with acromesomelic hypomineralization and campomelia in siblings.
    Kannu P, McFarlane JH, Savarirayan R, Aftimos S.
    Am J Med Genet A; 2007 Nov 01; 143A(21):2607-11. PubMed ID: 17935248
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  • 33. Two female siblings with congenital heart disease, postaxial polydactyly, ectopic neuropituitary gland, hair anomalies and characteristic facial features: a new syndrome?
    Goossens L, Janssens S, Meersschaut V, Peeters H, Devlieger H, Devriendt K.
    Clin Dysmorphol; 2006 Apr 01; 15(2):71-4. PubMed ID: 16531731
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  • 34. Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome.
    Frank V, den Hollander AI, Brüchle NO, Zonneveld MN, Nürnberg G, Becker C, Du Bois G, Kendziorra H, Roosing S, Senderek J, Nürnberg P, Cremers FP, Zerres K, Bergmann C.
    Hum Mutat; 2008 Jan 01; 29(1):45-52. PubMed ID: 17705300
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  • 35. The Meckel syndrome: report of two Japanese sibs and a review of literature.
    Sugiura Y, Suzuki Y, Kobayashi M.
    Am J Med Genet; 1996 May 31; 67(3):312-4. PubMed ID: 8725749
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  • 40. Perlman syndrome: report of a case with additional radiographic findings.
    Herman TE, McAlister WH.
    Pediatr Radiol; 1995 Nov 31; 25 Suppl 1():S70-2. PubMed ID: 8577560
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