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Journal Abstract Search

517 related items for PubMed ID: 28302550

  • 1. The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon.
    Wonkam A, Toko R, Chelo D, Tekendo-Ngongang C, Kingue S, Dahoun S.
    Glob Heart; 2017 Jun; 12(2):115-120. PubMed ID: 28302550
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  • 3. Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion.
    Rakonjac M, Cuturilo G, Stevanovic M, Jelicic L, Subotic M, Jovanovic I, Drakulic D.
    Res Dev Disabil; 2016 Aug; 55():322-9. PubMed ID: 27235769
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  • 5. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects.
    Hou JW, Wang JK, Tsai WY, Chou CC, Wang TR.
    J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164
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  • 6. [22q11.2 deletion syndrome and complex congenital heart defects].
    Rosa RF, Trevisan P, Koshiyama DB, Pilla CB, Zen PR, Varella-Garcia M, Paskulin GA.
    Rev Assoc Med Bras (1992); 2011 Jun; 57(1):62-5. PubMed ID: 21390462
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  • 7. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.
    Iserin L, de Lonlay P, Viot G, Sidi D, Kachaner J, Munnich A, Lyonnet S, Vekemans M, Bonnet D.
    Eur J Pediatr; 1998 Nov; 157(11):881-4. PubMed ID: 9835429
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  • 8. 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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  • 10. Prevalence of chromosomal abnormalities and 22q11.2 deletion in conotruncal and non-conotruncal antenatally diagnosed congenital heart diseases in a Chinese population.
    Kong CW, Cheng YKY, To WWK, Leung TY.
    Hong Kong Med J; 2019 Feb; 25(1):6-12. PubMed ID: 30655461
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  • 12. 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin.
    Fokstuen S, Arbenz U, Artan S, Dutly F, Bauersfeld U, Brecevic L, Fasnacht M, Röthlisberger B, Schinzel A.
    Clin Genet; 1998 Jan; 53(1):63-9. PubMed ID: 9550365
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  • 15. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL, Chen CP, Wang LK, Ko TM, Chang TY, Chern SR, Wu PS, Chen YT, Chang SY.
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
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  • 17. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.
    Botto LD, May K, Fernhoff PM, Correa A, Coleman K, Rasmussen SA, Merritt RK, O'Leary LA, Wong LY, Elixson EM, Mahle WT, Campbell RM.
    Pediatrics; 2003 Jul; 112(1 Pt 1):101-7. PubMed ID: 12837874
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  • 19. Tricuspid atresia and 22q11 deletion.
    Marino B, Digilio MC, Novelli G, Giannotti A, Dallapiccola B.
    Am J Med Genet; 1997 Oct 03; 72(1):40-2. PubMed ID: 9295072
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  • 20. [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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