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Journal Abstract Search


375 related items for PubMed ID: 12975788

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  • 24. [Prenatal diagnosis of heart defects and associated chromosomal aberrations].
    Chaoui R, Körner H, Bommer C, Göldner B, Bierlich A, Bollmann R.
    Ultraschall Med; 1999 Oct; 20(5):177-84. PubMed ID: 10595385
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  • 26. Fetal right aortic arch: associated anomalies, genetic anomalies with chromosomal microarray analysis, and postnatal outcome.
    Peng R, Xie HN, Zheng J, Zhou Y, Lin MF.
    Prenat Diagn; 2017 Apr; 37(4):329-335. PubMed ID: 28165153
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  • 27. 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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  • 30. Prenatal diagnosis of congenital heart disease in the Naples area during the years 1994-1999 -- the experience of a joint fetal-pediatric cardiology unit.
    Paladini D, Russo M, Teodoro A, Pacileo G, Capozzi G, Martinelli P, Nappi C, Calabrò R.
    Prenat Diagn; 2002 Jul; 22(7):545-52. PubMed ID: 12124685
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  • 34. Chromosomal abnormalities among children born with conotruncal cardiac defects.
    Lammer EJ, Chak JS, Iovannisci DM, Schultz K, Osoegawa K, Yang W, Carmichael SL, Shaw GM.
    Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):30-5. PubMed ID: 19067405
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  • 35. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.
    Driscoll DA, Salvin J, Sellinger B, Budarf ML, McDonald-McGinn DM, Zackai EH, Emanuel BS.
    J Med Genet; 1993 Oct; 30(10):813-7. PubMed ID: 8230155
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