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Journal Abstract Search

347 related items for PubMed ID: 16700088

  • 1. 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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  • 2. Molecular characterization of a ring chromosome 15 in a fetus with intra uterine growth retardation and diaphragmatic hernia.
    Hatem E, Meriam BR, Walid D, Adenen M, Moez G, Ali S.
    Prenat Diagn; 2007 May; 27(5):471-4. PubMed ID: 17380471
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  • 3. Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.
    Wu BL, Schneider GH, Sabatino DE, Bozovic LZ, Cao B, Korf BR.
    Am J Med Genet; 1996 Mar 01; 62(1):77-83. PubMed ID: 8779331
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  • 4. Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1-15q26.2.
    Slavotinek AM, Moshrefi A, Davis R, Leeth E, Schaeffer GB, Burchard GE, Shaw GM, James B, Ptacek L, Pennacchio LA.
    Eur J Hum Genet; 2006 Sep 01; 14(9):999-1008. PubMed ID: 16736036
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  • 6. Prenatal detection and mapping of a distal 8p deletion associated with congenital heart disease.
    Bhatia SN, Suri V, Bundy A, Krauss CM.
    Prenat Diagn; 1999 Sep 01; 19(9):863-7. PubMed ID: 10521847
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  • 9. A fetus diagnosed with Casamassima-Morton-Nance syndrome with de novo del(8)(p23.1).
    Sasaki A, Hayashi S, Oi R, Anami A, Hanaoka M, Miyazaki O, Matsuoka K, Sago H.
    Prenat Diagn; 2011 Apr 01; 31(4):407-9. PubMed ID: 21413036
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  • 12. Congenital diaphragmatic hernia (CDH) etiology as revealed by pathway genetics.
    Kantarci S, Donahoe PK.
    Am J Med Genet C Semin Med Genet; 2007 May 15; 145C(2):217-26. PubMed ID: 17436295
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  • 14. Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects.
    Keitges EA, Pasion R, Burnside RD, Mason C, Gonzalez-Ruiz A, Dunn T, Masiello M, Gebbia JA, Fernandez CO, Risheg H.
    Am J Med Genet A; 2013 Jul 15; 161A(7):1755-8. PubMed ID: 23696316
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  • 16. [Risk of missed diagnosis of 22q11.2 deletion in a fetal cardiac conotruncal malformation when another chromosomal abnormality is detected].
    Picone O, Brisset S, Senat MV, Maurin ML, Frydman R, Tachdjian G.
    J Gynecol Obstet Biol Reprod (Paris); 2008 May 15; 37(3):299-301. PubMed ID: 18160230
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  • 17. Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1.
    Slavotinek A, Lee SS, Davis R, Shrit A, Leppig KA, Rhim J, Jasnosz K, Albertson D, Pinkel D.
    J Med Genet; 2005 Sep 15; 42(9):730-6. PubMed ID: 16141010
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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 15; 28(6):534-7. PubMed ID: 10598346
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  • 19. Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect.
    Jaillard S, Loget P, Lucas J, Dubourg C, Le Bouar G, Demurger F, Bertorello I, David V, Poulain P, Odent S, Belaud-Rotureau MA.
    Eur J Med Genet; 2011 Oct 15; 54(2):186-8. PubMed ID: 21115145
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  • 20. Deletion 15q24-26 in prenatally detected diaphragmatic hernia: increasing evidence of a candidate region for diaphragmatic development.
    Schlembach D, Zenker M, Trautmann U, Ulmer R, Beinder E.
    Prenat Diagn; 2001 Apr 15; 21(4):289-92. PubMed ID: 11288119
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