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Journal Abstract Search

318 related items for PubMed ID: 16222476

  • 1. Differential detection of deletion 22q11.2 syndrome by specialty and indication.
    Katzman PJ, Wang B, Sawhney M, Wang N.
    Pediatr Dev Pathol; 2005; 8(5):557-67. PubMed ID: 16222476
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  • 2. Chromosome 22q11.2 microdeletions in velocardiofacial syndrome patients with widely variable manifestations.
    Ravnan JB, Chen E, Golabi M, Lebo RV.
    Am J Med Genet; 1996 Dec 18; 66(3):250-6. PubMed ID: 8985481
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  • 4. [Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome].
    Pânzaru M, Rusu C, Voloşciuc M, Braha E, Butnariu L, Ivanov I, Grămescu M, Popescu R, Caba L, Sireteanu A, Macovei M, Covic M, Gorduza EV.
    Rev Med Chir Soc Med Nat Iasi; 2011 Dec 18; 115(3):756-61. PubMed ID: 22046783
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  • 9. Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
    Kitsiou-Tzeli S, Kolialexi A, Fryssira H, Galla-Voumvouraki A, Salavoura K, Kanariou M, Tsangaris GT, Kanavakis E, Mavrou A.
    In Vivo; 2004 Dec 18; 18(5):603-8. PubMed ID: 15523900
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  • 10. Clinical correlation of chromosome 22q11.2 fluorescent in situ hybridization analysis and velocardiofacial syndrome.
    Oh AK, Workman LA, Wong GB.
    Cleft Palate Craniofac J; 2007 Jan 18; 44(1):62-6. PubMed ID: 17214538
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  • 12. Use of FISH technique in the diagnosis of chromosomal syndromes.
    Iqbal MA, Ulmer C, Sakati N.
    East Mediterr Health J; 1999 Nov 18; 5(6):1218-24. PubMed ID: 11924115
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  • 14. Chromosome 22q11 deletions in patients with selected outflow tract malformations.
    Frohn-Mulder IM, Wesby Swaay E, Bouwhuis C, Van Hemel JO, Gerritsma E, Niermeyer MF, Hess J.
    Genet Couns; 1999 Nov 18; 10(1):35-41. PubMed ID: 10191427
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  • 16. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G, Alvares S, Rocha C, Teixeira MF, Mota MC, Reis MI, Feijó MJ, Lima MR, Pinto MR.
    Rev Port Cardiol; 2005 Mar 18; 24(3):349-71. PubMed ID: 15929620
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  • 20. The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndrome.
    Van Esch H, Groenen P, Fryns JP, Van de Ven W, Devriendt K.
    Genet Couns; 1999 Mar 18; 10(1):59-65. PubMed ID: 10191430
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