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Journal Abstract Search

142 related items for PubMed ID: 11343338

  • 21. Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection.
    Delatycki MB, Voullaire L, Francis D, Petrovic V, Robertson A, Webber LM, Slater HR.
    J Med Genet; 1999 Apr; 36(4):335-8. PubMed ID: 10227406
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  • 22. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
    Kato R, Kishibayashi J, Shimokawa O, Harada N, Niikawa N, Matsumoto N.
    Am J Med Genet; 2001 Dec 15; 104(4):319-22. PubMed ID: 11754068
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  • 23. Subtelomeric rearrangements in mental retardation: Hacettepe University experience in 130 patients.
    Utine GE, Celik T, Alanay Y, Alikaşifoğlu M, Boduroğlu K, Tunçbilek E, Aktaş D.
    Turk J Pediatr; 2009 Dec 15; 51(3):199-206. PubMed ID: 19817261
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  • 24. Trisomy 2p: analysis of unusual phenotypic findings.
    Lurie IW, Ilyina HG, Gurevich DB, Rumyantseva NV, Naumchik IV, Castellan C, Hoeller A, Schinzel A.
    Am J Med Genet; 1995 Jan 16; 55(2):229-36. PubMed ID: 7717424
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  • 25. Partial monosomy 2p and partial trisomy 4q due to paternal translocation t(2;4)(p25.1;q31.3).
    Skrlec I, Wagner J, Puseljić S, Heffer M, Stipoljev F.
    Coll Antropol; 2014 Jun 16; 38(2):759-62. PubMed ID: 25145019
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  • 26. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M, Hemly NA, Zaki MS.
    Genet Couns; 2007 Jun 16; 18(2):217-26. PubMed ID: 17710874
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  • 27. M-FISH applications in clinical genetics.
    Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G.
    Genet Couns; 2005 Jun 16; 16(3):257-68. PubMed ID: 16259323
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  • 28. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP, Chern SR, Wang TH, Hsueh DW, Lee CC, Town DD, Wang W, Ko TM.
    Prenat Diagn; 2005 Jun 16; 25(6):492-6. PubMed ID: 15966044
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  • 30. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
    Chen CP, Chern SR, Wang W, Lee CC, Chen WL, Chen LF, Chang TY, Tzen CY.
    Prenat Diagn; 2001 May 16; 21(5):346-50. PubMed ID: 11360273
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  • 35. Trisomy 2p syndrome: a fetus with anencephaly and postaxial polydactyly.
    Hahm GK, Barth RF, Schauer GM, Reiss R, Opitz JM.
    Am J Med Genet; 1999 Nov 05; 87(1):45-8. PubMed ID: 10528246
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  • 36. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
    Szabó Gabriella P, Balogh E, Jakab Z, Germán P, Bodnár F, Kiss A, Telek B, Oláh E.
    Orv Hetil; 2002 Dec 15; 143(50):2775-9. PubMed ID: 12583317
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  • 37. Precocious puberty associated with partial trisomy 18q and monosomy 11q.
    Mutesa L, Hellin AC, Jamar M, Pierquin G, Bours V, Verloes A.
    Genet Couns; 2007 Dec 15; 18(2):201-7. PubMed ID: 17710872
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  • 39. Partial distal trisomy 3p. A partial autosomal trisomy without major dysmorphic features.
    Smeets E, Vandenbossche L, Fryns JP.
    Genet Couns; 2001 Dec 15; 12(1):85-9. PubMed ID: 11332982
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