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Journal Abstract Search

254 related items for PubMed ID: 1466569

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  • 5. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
    Courtens W, Wuyts W, Scheers S, Van Luijk R, Reyniers E, Rooms L, Ceulemans B, Kooy F, Wauters J.
    Eur J Med Genet; 2006; 49(5):402-13. PubMed ID: 16488200
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  • 6. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
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  • 7. 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; 18(2):201-7. PubMed ID: 17710872
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  • 8. Combined 10pter-->p11 and 18pter-->q11 trisomy in a 7-year-old child.
    Lapière JC, Verloes A, Herens C, Delfortrie J, Van Maldergem L, Gillerot Y, Koulischer L.
    Genet Couns; 1992; 3(3):155-9. PubMed ID: 1388935
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  • 9. [Partial trisomy 18q].
    Darnaude MT, López Pajares I, Delicado A, García Frias E.
    An Esp Pediatr; 1987 Jun; 26(6):460-2. PubMed ID: 3631780
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  • 13. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
    Kupchik GS, Barrett SK, Babu A, Charria-Ortiz G, Velinov M, Macera MJ.
    Eur J Med Genet; 2005 Jun; 48(1):57-65. PubMed ID: 15953407
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  • 15. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J, Chernos J, Roland B.
    Am J Med Genet; 1997 Dec 19; 73(3):327-9. PubMed ID: 9415693
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  • 16. [Proximal monosomy 13].
    Geormăneanu M, Geormăneanu C.
    Ann Genet; 1990 Dec 19; 33(3):176-8. PubMed ID: 2288464
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  • 17. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
    Rao VB, Kerketta L, Korgaonkar S, Ghosh K, Mohanty D.
    Genet Couns; 2005 Dec 19; 16(2):139-43. PubMed ID: 16082769
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  • 18. [Partial 11q trisomy due to missegregation of maternal t(11;22) (q23;q11.1) translocation (author's transl)].
    Pangalos C, Couturier J, Bartsocas C, Theodorou S.
    Nouv Presse Med; 1980 Nov 01; 9(41):3065-7. PubMed ID: 7443445
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  • 19. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
    Grammatico P, Majore S, Marrocco G, Poscente M, Mordenti C, Grammatico B, Del Porto G.
    Genet Couns; 1999 Nov 01; 10(4):351-8. PubMed ID: 10631922
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  • 20. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11).
    Murthy DS, Patel ZM, Ambani LM.
    Clin Genet; 1980 Oct 01; 18(4):233-8. PubMed ID: 7438504
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