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Journal Abstract Search

240 related items for PubMed ID: 8669450

  • 21. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
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  • 22. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP, Su YN, Chern SR, Hsu CY, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
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  • 23. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H, Vermeesch J, Fryns JP.
    Genet Couns; 2008 Mar; 19(4):365-71. PubMed ID: 19239079
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  • 25. Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome.
    Bergman A, Blennow E.
    Eur J Hum Genet; 2000 Oct; 8(10):801-4. PubMed ID: 11039583
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  • 26. Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.
    Cheng SD, Spinner NB, Zackai EH, Knoll JH.
    Am J Hum Genet; 1994 Oct; 55(4):753-9. PubMed ID: 7942854
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  • 27. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
    Zenger-Hain JL, Van Dyke DL, Wiktor A, Walker H, Feldman GL.
    Am J Med Genet; 1993 Dec 01; 47(8):1198-201. PubMed ID: 8291556
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  • 28. The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings.
    Buoni S, Sorrentino L, Farnetani MA, Pucci L, Fois A.
    J Child Neurol; 2000 Jun 01; 15(6):380-5. PubMed ID: 10868780
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  • 29. Molecular cytogenetic characterization of a small, familial supernumerary ring chromosome 7 associated with mental retardation and an abnormal phenotype.
    Tan-Sindhunata G, Castedo S, Leegte B, Mulder I, vd Veen AY, vd Hout AH, Wiersma TJ, van Essen AJ.
    Am J Med Genet; 2000 May 15; 92(2):147-52. PubMed ID: 10797441
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  • 32. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO, Karauzum SB, Mihci E, Tacoy S, Luleci G.
    Genet Couns; 2005 May 15; 16(2):129-38. PubMed ID: 16080292
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  • 37. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L, Recalcati MP, Bedeschi MF, Lalatta F, Valtorta C, Bellini M, Finelli P, Larizza L, Giardino D.
    Eur J Med Genet; 2009 May 15; 52(4):218-23. PubMed ID: 19236961
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  • 39. Inv dup (15): is the electroclinical phenotype helpful for this challenging clinical diagnosis?
    Valente KD, Freitas A, Fridman C, Varela M, Silva AE, Fett AC, Koiffmann CP.
    Clin Neurophysiol; 2006 Apr 15; 117(4):803-9. PubMed ID: 16495142
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  • 40. Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.
    Long FL, Duckett DP, Billam LJ, Williams DK, Crolla JA.
    J Med Genet; 1998 May 15; 35(5):425-8. PubMed ID: 9610809
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