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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

173 related items for PubMed ID: 7523003

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  • 4. Cobblestone-like brain dysgenesis and altered glycosylation in congenital cutis laxa, Debre type.
    Van Maldergem L, Yuksel-Apak M, Kayserili H, Seemanova E, Giurgea S, Basel-Vanagaite L, Leao-Teles E, Vigneron J, Foulon M, Greally M, Jaeken J, Mundlos S, Dobyns WB.
    Neurology; 2008 Nov 11; 71(20):1602-8. PubMed ID: 18716235
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  • 5. Male with type II autosomal recessive cutis laxa.
    Imaizumi K, Kurosawa K, Makita Y, Masuno M, Kuroki Y.
    Clin Genet; 1994 Jan 11; 45(1):40-3. PubMed ID: 8149651
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  • 19. Dandy-Walker malformation in the Meckel syndrome.
    Herriot R, Hallam LA, Gray ES.
    Am J Med Genet; 1991 May 01; 39(2):207-10. PubMed ID: 2063927
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  • 20. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML, Ryan RM.
    Am J Med Genet; 1995 Mar 13; 56(1):97-100. PubMed ID: 7747796
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