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Journal Abstract Search

227 related items for PubMed ID: 10227406

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  • 3. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
    Senger G, Chudoba I, Friedrich U, Tommerup N, Claussen U, Brøndum-Nielsen K.
    Prenat Diagn; 1997 Apr; 17(4):369-74. PubMed ID: 9160390
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  • 4. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
    Ausems MG, Schuil J, Van Raveswaaij-Arts C, De Pater JM.
    Genet Couns; 2004 Apr; 15(4):405-10. PubMed ID: 15658615
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  • 6. [Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human].
    Karamysheva TV, Matveeva VG, Shorina AP, Rubtsov NB.
    Genetika; 2001 Jun; 37(6):811-6. PubMed ID: 11517768
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  • 12. Duplication of chromosome region 8p23.1-->p23.3: a benign variant?
    Engelen JJ, Moog U, Evers JL, Dassen H, Albrechts JC, Hamers AJ.
    Am J Med Genet; 2000 Mar 06; 91(1):18-21. PubMed ID: 10751083
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  • 13. Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.
    Wanderley HY, Schrander-Stumpel CT, Visser MO, Van Maanen-Op Het Roodt EA, Loneus WH, Engelen JJ.
    Genet Couns; 2005 Mar 06; 16(3):277-82. PubMed ID: 16259325
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  • 14. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
    Mach M, Windpassinger C, Wagner K, Kroisel PM, Petek E.
    Genet Couns; 2007 Mar 06; 18(1):9-16. PubMed ID: 17515297
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  • 15. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
    Vásquez-Velásquez AI, García-Castillo HA, González-Mercado MG, Dávalos IP, Raca G, Xu X, Dwyer E, Rivera H.
    Cytogenet Genome Res; 2011 Mar 06; 132(4):233-8. PubMed ID: 21063078
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  • 17. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Huang JK, Lee CC, Wang W.
    Genet Couns; 2006 Mar 06; 17(1):57-63. PubMed ID: 16719278
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  • 19. Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.
    Fritz B, Müller-Navia J, Hillig U, Köhler M, Aslan M, Rehder H.
    Am J Med Genet; 1999 Dec 03; 87(4):297-301. PubMed ID: 10588833
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  • 20. Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality.
    Tonk V, Schneider NR, Delgado MR, Mao J, Schultz RA.
    Am J Med Genet; 1996 Jan 02; 61(1):16-20. PubMed ID: 8741911
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