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Journal Abstract Search

284 related items for PubMed ID: 11850602

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  • 4. [Prenatal diagnosis of 22q11 microdeletion syndrome].
    Cai M, Huang H, Lin N, Guo N, Wu X, Su L, Xu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr 10; 34(2):192-195. PubMed ID: 28397216
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  • 5. 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 10; 85(1):30-5. PubMed ID: 19067405
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  • 10. Prenatal detection of a tetralogy of Fallot with origin of the left pulmonary artery from the ascending aorta in a familial 22q11 microdeletion.
    Saliba Z, Le Bidois J, Sidi D, Kachaner J, Bonnet D.
    Prenat Diagn; 1999 Mar 10; 19(3):260-2. PubMed ID: 10210126
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  • 11. 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 10; 53(2):248-51. PubMed ID: 25017279
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  • 13. 22q11.2 microdeletions in adults with familial tetralogy of Fallot.
    Hokanson JS, Pierpont E, Hirsch B, Moller JH.
    Genet Med; 2001 Jun 10; 3(1):61-4. PubMed ID: 11339381
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  • 16. Chromosome 22q11 microdeletions in tetralogy of Fallot.
    Trainer AH, Morrison N, Dunlop A, Wilson N, Tolmie J.
    Arch Dis Child; 1996 Jan 10; 74(1):62-3. PubMed ID: 8660052
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