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538 related items for PubMed ID: 17121426

  • 1. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
    Chen M, Hwu WL, Kuo SJ, Chen CP, Yin PL, Chang SP, Lee DJ, Chen TH, Wang BT, Lin CC.
    Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
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  • 3. Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis.
    Iqbal MA, Ramadan S, Ali FA, Kurdi W.
    Prenat Diagn; 2005 Dec; 25(12):1142-9. PubMed ID: 16240463
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  • 6. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP, Devriendt K, Chern SR, Lee CC, Wang W, Lin SP.
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
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  • 8. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W.
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
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  • 9. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
    Hsieh LJ, Hsieh TC, Yeh GP, Lin MI, Chen M, Wang BB.
    Fetal Diagn Ther; 2004 Apr; 19(4):356-60. PubMed ID: 15192296
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  • 10. Incidences of micro-deletion/duplication 22q11.2 detected by multiplex ligation-dependent probe amplification in patients with congenital cardiac disease who are scheduled for cardiac surgery.
    Hu Y, Zhu X, Yang Y, Mo X, Sheng M, Yao J, Wang D.
    Cardiol Young; 2009 Apr; 19(2):179-84. PubMed ID: 19224675
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  • 11. Subtelomeric rearrangements: results from FISH studies in 84 families with idiopathic mental retardation.
    Bocian E, Hélias-Rodzewicz Z, Suchenek K, Obersztyn E, Kutkowska-Kaźmierczak A, Stankiewicz P, Kostyk E, Mazurczak T.
    Med Sci Monit; 2004 Apr; 10(4):CR143-51. PubMed ID: 15039644
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  • 12. Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods.
    Erjavec-Skerget A, Stangler-Herodez S, Zagorac A, Zagradisnik B, Kokalj-Vokac N.
    Croat Med J; 2006 Dec; 47(6):841-50. PubMed ID: 17167856
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  • 13. Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective study.
    Boudjemline Y, Fermont L, Le Bidois J, Lyonnet S, Sidi D, Bonnet D.
    J Pediatr; 2001 Apr; 138(4):520-4. PubMed ID: 11295715
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  • 14. Congenital heart defects and chromosomal anomalies including 22q11 microdeletion (CATCH 22).
    Soares G, Alvares S, Rocha C, Teixeira MF, Mota MC, Reis MI, Feijó MJ, Lima MR, Pinto MR.
    Rev Port Cardiol; 2005 Mar; 24(3):349-71. PubMed ID: 15929620
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  • 15. Prenatal diagnosis of de novo deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects.
    López I, Bafalliu JA, Bernabé MC, García F, Costa M, Guillén-Navarro E.
    Prenat Diagn; 2006 Jun; 26(6):577-80. PubMed ID: 16700088
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  • 16. Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization.
    Cogulu O, Gunduz C, Karaca E, Onay H, Ozkinay C, Ozkinay F.
    Genet Couns; 2006 Jun; 17(3):321-31. PubMed ID: 17100201
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  • 17. Array comparative genomic hybridization in prenatal diagnosis: another experience.
    Vialard F, Molina Gomes D, Leroy B, Quarello E, Escalona A, Le Sciellour C, Serazin V, Roume J, Ville Y, de Mazancourt P, Selva J.
    Fetal Diagn Ther; 2009 Jun; 25(2):277-84. PubMed ID: 19521095
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  • 18. [Microdeletion of 22q11 and conotruncal cardiopathies: contribution of prenatal diagnosis].
    Verspyck E, Joly G, Rossi A, David N, Blaysat G, Henocq A, Moirot H, Labadie G, Marpeau L.
    J Gynecol Obstet Biol Reprod (Paris); 1999 Oct; 28(6):534-7. PubMed ID: 10598346
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