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Journal Abstract Search

1280 related items for PubMed ID: 17295158

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  • 4. Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
    Beauchesne LM, Warnes CA, Connolly HM, Ammash NM, Grogan M, Jalal SM, Michels VV.
    J Am Coll Cardiol; 2005 Feb 15; 45(4):595-8. PubMed ID: 15708709
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  • 5. Congenital cardiac defects with 22q11 deletion.
    Giray O, Ulgenalp A, Bora E, Sağin Saylam G, Unal N, Meşe T, Hüdaoğlu S, Erçal D.
    Turk J Pediatr; 2003 Feb 15; 45(3):217-20. PubMed ID: 14696799
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  • 8. CATCH 22 syndrome: report of 7 infants with follow-up data and review of the recent advancements in the genetic knowledge of the locus 22q11.
    Sergi C, Serpi M, Müller-Navia J, Schnabel PA, Hagl S, Otto HF, Ulmer HE.
    Pathologica; 1999 Jun 15; 91(3):166-72. PubMed ID: 10536461
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  • 10. [Chromosome 22 (22q.11.2) deletion. Etiology of conotruncal heart abnormalities].
    Buendía Hernández A, Calderón-Colmenero J, Aizpuru E, Attie CL, Zabal C, Patiño E, Miranda I, Juanico A, Attie F.
    Arch Inst Cardiol Mex; 2000 Jun 15; 70(2):148-53. PubMed ID: 10932799
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  • 11. Kousseff syndrome caused by deletion of chromosome 22q11-13.
    Forrester S, Kovach MJ, Smith RE, Rimer L, Wesson M, Kimonis VE.
    Am J Med Genet; 2002 Nov 01; 112(4):338-42. PubMed ID: 12376934
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  • 12. Screening of patients at risk for 22q11 deletion.
    Barisić I, Morozin Pohovski L, Petković I, Cvetko Z, Stipancić G, Bagatin M.
    Coll Antropol; 2008 Mar 01; 32(1):165-9. PubMed ID: 18494202
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  • 13. Velo-cardio-facial syndrome: frequency and extent of 22q11 deletions.
    Lindsay EA, Goldberg R, Jurecic V, Morrow B, Carlson C, Kucherlapati RS, Shprintzen RJ, Baldini A.
    Am J Med Genet; 1995 Jul 03; 57(3):514-22. PubMed ID: 7677167
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  • 14. [Study on clinical features and fluorescence in situ hybridization detections of 22q11 microdeletion syndrome].
    Qin YF, Yang JB, Xie CH, Shao J, Zhao ZY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun 03; 24(3):284-7. PubMed ID: 17557238
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  • 15. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
    McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH.
    Genet Couns; 1999 Jun 03; 10(1):11-24. PubMed ID: 10191425
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  • 17. Differential detection of deletion 22q11.2 syndrome by specialty and indication.
    Katzman PJ, Wang B, Sawhney M, Wang N.
    Pediatr Dev Pathol; 2005 Jun 03; 8(5):557-67. PubMed ID: 16222476
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  • 18. [Relationship between 22q11 microdeletion syndrome and congenital heart disease].
    Qin YF, Xie CH, Yang JB, Wu DW, Shao J, Zhao ZY.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2011 Jul 03; 39(7):631-5. PubMed ID: 22088244
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  • 19. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
    Vantrappen G, Rommel N, Devriendt K, Cremers CW, Feenstra L, Fryns JP.
    Acta Otorhinolaryngol Belg; 2001 Jul 03; 55(1):43-8. PubMed ID: 11256191
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