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Journal Abstract Search

364 related items for PubMed ID: 18494202

  • 1. 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; 32(1):165-9. PubMed ID: 18494202
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  • 2. Microdeletion 22q11 and oesophageal atresia.
    Digilio MC, Marino B, Bagolan P, Giannotti A, Dallapiccola B.
    J Med Genet; 1999 Feb; 36(2):137-9. PubMed ID: 10051013
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  • 3. Genetic background of congenital conotruncal heart defects--a study of 45 families.
    Kwiatkowska J, Wierzba J, Aleszewicz-Baranowska J, Ereciński J.
    Kardiol Pol; 2007 Jan; 65(1):32-7; discussion 38-9. PubMed ID: 17295158
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  • 5. 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; 91(3):166-72. PubMed ID: 10536461
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  • 6. Under-recognition of 22q11.2 deletion in adult Chinese patients with conotruncal anomalies: implications in transitional care.
    Liu AP, Chow PC, Lee PP, Mok GT, Tang WF, Lau ET, Lam ST, Chan KY, Kan AS, Chau AK, Cheung YF, Lau YL, Chung BH.
    Eur J Med Genet; 2014 Jun; 57(6):306-11. PubMed ID: 24721633
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  • 9. Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence.
    McDonald-McGinn DM, Driscoll DA, Emanuel BS, Goldmuntz E, Clark BJ, Solot C, Cohen M, Schultz P, LaRossa D, Randall P, Zackai EH.
    Pediatrics; 1997 May; 99(5):E9. PubMed ID: 9113966
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  • 10. Catch 22--microdeletion 22q11 screening in patients with congenital heart defects.
    Von Beust G, Bartmus D, Bartels I.
    Genet Couns; 1998 May; 9(3):223-7. PubMed ID: 9777346
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  • 12. Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland.
    Wozniak A, Wolnik-Brzozowska D, Wisniewska M, Glazar R, Materna-Kiryluk A, Moszura T, Badura-Stronka M, Skolozdrzy J, Krawczynski MR, Zeyland J, Bobkowski W, Slomski R, Latos-Bielenska A, Siwinska A.
    BMC Pediatr; 2010 Dec 06; 10():88. PubMed ID: 21134246
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  • 14. [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 06; 115(3):756-61. PubMed ID: 22046783
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  • 15. [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 06; 39(7):631-5. PubMed ID: 22088244
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