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Journal Abstract Search

78 related items for PubMed ID: 3777028

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  • 2. Split-foot anomaly, microphthalmia, cleft-lip and cleft-palate, and mental retardation associated with a chromosome 6;13 translocation.
    Viljoen DL, Smart R.
    Clin Dysmorphol; 1993 Jul; 2(3):274-7. PubMed ID: 8287191
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  • 6. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
    Cai T, Yu P, Tagle DA, Xia J.
    Am J Med Genet; 1999 Oct 08; 86(4):305-11. PubMed ID: 10494083
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  • 8. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome.
    Kitsiou-Tzeli S, Hallett JJ, Atkins L, Latt SA, Holmes LB.
    Am J Med Genet; 1984 Aug 08; 18(4):725-9. PubMed ID: 6237580
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  • 10. Cohen syndrome and de novo reciprocal translocation t(5;7)(q33.1;p15.1).
    Fryns JP, Kleczkowska A, Smeets E, Thiry P, Geutjens J, Van den Berghe H.
    Am J Med Genet; 1990 Dec 08; 37(4):546-7. PubMed ID: 2260606
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  • 13. De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.
    Curotti G, Benkhalifa M, Raybaud C, Picard F, Bellec V, Qumsiyeh MB.
    Genet Couns; 1999 Dec 08; 10(3):259-64. PubMed ID: 10546097
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  • 14. Anterior chamber eye anomalies, redundant skin and syndactyly--a new syndrome associated with breakpoints at 2q37.2 and 7q36.3.
    Temple IK, Browne C, Hodgkins P.
    Clin Dysmorphol; 1999 Jul 08; 8(3):157-63. PubMed ID: 10457847
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  • 16. De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.
    Riegel M, Baumer A, Piram A, Ortolan D, Peres LC, Pina-Neto JM.
    Genet Couns; 2001 Jul 08; 12(1):69-75. PubMed ID: 11332980
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  • 17. Smith-Lemli-Opitz syndrome in a female with a de novo, balanced translocation involving 7q32: probable disruption of an SLOS gene.
    Wallace M, Zori RT, Alley T, Whidden E, Gray BA, Williams CA.
    Am J Med Genet; 1994 May 01; 50(4):368-74. PubMed ID: 8209918
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  • 20. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 01; 26(2):138-46. PubMed ID: 16470734
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