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Journal Abstract Search

608 related items for PubMed ID: 7645598

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  • 3. Partial trisomy and partial monosomy of the distal long arm of chromosome 4: patient report and literature review.
    Frints SG, Schrander-Stumpel CT, Engelen JJ, Da Costa AJ, Fryns JP.
    Genet Couns; 1996; 7(2):135-42. PubMed ID: 8831133
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  • 5. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
    Okada M, Usami A, Okajima K, Yamada M, Yamaguchi Y, Umezaki I, Matsuda Y, Ohta H.
    Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
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  • 6. Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.
    Cohn AC, Kearns LS, Savarirayan R, Ryan J, Craig JE, Mackey DA.
    Ophthalmic Genet; 2005 Mar; 26(1):45-53. PubMed ID: 15823925
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  • 9. DiGeorge syndrome and partial monosomy 10p: case report and review.
    Schuffenhauer S, Seidel H, Oechsler H, Belohradsky B, Bernsau U, Murken J, Meitinger T.
    Ann Genet; 1995 Mar; 38(3):162-7. PubMed ID: 8540688
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  • 10. Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay.
    Chen CP, Lin SP, Chen MR, Su YN, Chern SR, Liu YP, Su JW, Lee MS, Wang W.
    Genet Couns; 2012 Mar; 23(3):405-13. PubMed ID: 23072190
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  • 11. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A, Bova R, Bellanova G, Chindemi A, Zappata S, Brahe C.
    Am J Med Genet; 1997 Aug 08; 71(2):139-43. PubMed ID: 9217211
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  • 15. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.
    Quadrelli R, Quadrelli A, Milunsky A, Zou YS, Huang XL, Viera E, Mechoso B, Bellini S, Costabel M, Vaglio A.
    Genet Test Mol Biomarkers; 2009 Jun 08; 13(3):387-93. PubMed ID: 19473082
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  • 16. Duplication of part of chromosome 1q: clinical report and review of literature.
    Michels VV, Berseth CL, O'Brien JF, Dewald G.
    Am J Med Genet; 1984 May 08; 18(1):125-34. PubMed ID: 6430083
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  • 17. Phenotypic and cytogenetic spectrum of 9p trisomy.
    Temtamy SA, Kamel AK, Ismail S, Helmy NA, Aglan MS, El Gammal M, El Ruby M, Mohamed AM.
    Genet Couns; 2007 May 08; 18(1):29-48. PubMed ID: 17515299
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  • 18. Interstitial deletion of 8q21-->22 associated with minor anomalies, congenital heart defect, and Dandy-Walker variant.
    Donahue ML, Ryan RM.
    Am J Med Genet; 1995 Mar 13; 56(1):97-100. PubMed ID: 7747796
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  • 19. Characterization of a derivative chromosome 17 by fish-technique.
    Ramesh KH, Shah HO, Sherman J, Lin JH, Verma RS.
    Ann Genet; 1996 Mar 13; 39(3):177-80. PubMed ID: 8839891
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