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Journal Abstract Search

158 related items for PubMed ID: 9571276

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  • 4. Novel variants of ABCC9 in Japanese children with Cantú syndrome.
    Kubota K, Yamamoto T, Miyatake S, Matsumoto N, Fukao T.
    Pediatr Int; 2020 Mar; 62(3):410-412. PubMed ID: 32198910
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  • 5. Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).
    Lazalde B, Sánchez-Urbina R, Nuño-Arana I, Bitar WE, de Lourdes Ramírez-Dueñas M.
    Am J Med Genet; 2000 Oct 23; 94(5):421-7. PubMed ID: 11050630
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  • 7. Cantú syndrome as a rare cause of pericardial effusion in a young woman.
    Jesani H, Elangovan S, Zaidi A.
    Br J Hosp Med (Lond); 2019 Dec 02; 80(12):732-733. PubMed ID: 31822179
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  • 8. Multiple vascular anomalies and refractory pericardial effusion in a young patient with Cantu syndrome: a case report and review of the literature.
    Daas F, Gupta P, Kiblawi F.
    BMC Pediatr; 2023 Dec 19; 23(1):644. PubMed ID: 38114927
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  • 11. Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.
    Engels H, Bosse K, Ehrbrecht A, Zahn S, Hoischen A, Propping P, Bindl L, Reutter H.
    Am J Med Genet; 2002 Aug 01; 111(2):205-9. PubMed ID: 12210352
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  • 13. Cantu syndrome and lymphoedema.
    García-Cruz D, Mampel A, Echeverria MI, Vargas AL, Castañeda-Cisneros G, Davalos-Rodriguez N, Patiño-Garcia B, Garcia-Cruz MO, Castañeda V, Cardona EG, Marin-Solis B, Cantu JM, Nuñez-Reveles N, Moran-Moguel C, Thavanati PKR, Ramirez-Garcia S, Sanchez-Corona J.
    Clin Dysmorphol; 2011 Jan 01; 20(1):32-37. PubMed ID: 20890180
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  • 17. Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants.
    Kortüm F, Niceta M, Magliozzi M, Dumic Kubat K, Robertson SP, Moresco A, Dentici ML, Baban A, Leoni C, Onesimo R, Obregon MG, Digilio MC, Zampino G, Novelli A, Tartaglia M, Kutsche K.
    Eur J Med Genet; 2020 Sep 01; 63(9):103996. PubMed ID: 32622958
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  • 18. Cantú syndrome: report of nine new cases and expansion of the clinical phenotype.
    Scurr I, Wilson L, Lees M, Robertson S, Kirk E, Turner A, Morton J, Kidd A, Shashi V, Stanley C, Berry M, Irvine AD, Goudie D, Turner C, Brewer C, Smithson S.
    Am J Med Genet A; 2011 Mar 01; 155A(3):508-18. PubMed ID: 21344641
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  • 19. Dominant missense mutations in ABCC9 cause Cantú syndrome.
    Harakalova M, van Harssel JJ, Terhal PA, van Lieshout S, Duran K, Renkens I, Amor DJ, Wilson LC, Kirk EP, Turner CL, Shears D, Garcia-Minaur S, Lees MM, Ross A, Venselaar H, Vriend G, Takanari H, Rook MB, van der Heyden MA, Asselbergs FW, Breur HM, Swinkels ME, Scurr IJ, Smithson SF, Knoers NV, van der Smagt JJ, Nijman IJ, Kloosterman WP, van Haelst MM, van Haaften G, Cuppen E.
    Nat Genet; 2012 May 18; 44(7):793-6. PubMed ID: 22610116
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