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Journal Abstract Search

234 related items for PubMed ID: 8135272

  • 1. Monosomy 11q: report of two familial cases and review of the literature.
    Hustinx R, Verloes A, Grattagliano B, Herens C, Jamar M, Soyeur D, Schaaps JP, Koulischer L.
    Am J Med Genet; 1993 Sep 01; 47(3):312-7. PubMed ID: 8135272
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  • 2. Monosomy 11Q: report of new phenotypic manifestations.
    Puvabanditsin S, Garrow E, Zia-Ullah MO, Supavekin S, Lianthanasarn P, Denev KI.
    Genet Couns; 2001 Sep 01; 12(3):283-6. PubMed ID: 11693793
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  • 3. Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.
    Pettenati MJ, Teot LA, Smith C, Hayworth R, Thomas IT, Veille JC, Rao PN.
    Am J Med Genet; 1993 Feb 01; 45(3):365-9. PubMed ID: 8434625
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  • 4. Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndrome.
    Clementi M, Tenconi R, Turolla L, Silvan C, Bortotto L, Artifoni L.
    Am J Med Genet; 1991 Nov 01; 41(2):246-50. PubMed ID: 1785643
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  • 5. 11q- syndrome: three cases and a review of the literature.
    Leegte B, Kerstjens-Frederikse WS, Deelstra K, Begeer JH, van Essen AJ.
    Genet Couns; 1999 Nov 01; 10(3):305-13. PubMed ID: 10546104
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  • 6. Complex chromosome rearrangements and congenital anomalies.
    Kousseff BG, Nichols P, Essig YP, Miller K, Weiss A, Tedesco TA.
    Am J Med Genet; 1987 Apr 01; 26(4):771-82. PubMed ID: 3591822
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  • 7. Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1).
    Berry R, Wilson H, Robinson J, Sandlin C, Tyson W, Campbell J, Porreco R, Manchester D.
    Am J Med Genet; 1989 Nov 01; 34(3):358-65. PubMed ID: 2596525
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  • 8. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM, Sekhon GS, Laxova R.
    Am J Med Genet; 1994 Nov 15; 53(3):216-21. PubMed ID: 7856655
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  • 9. Duplication 7p in a family with t(7;11): association with anomalies of the anterior cranial base.
    Odell JM, Siebert JR, Bradley C, Salk D.
    Am J Med Genet; 1987 Jul 15; 27(3):687-92. PubMed ID: 3631140
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  • 12. 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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  • 13. Duplication of distal 22q.
    Abeliovich D, Maor E, Bashan N, Carmi R.
    Am J Med Genet; 1989 Mar 19; 32(3):346-9. PubMed ID: 2729354
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  • 17. 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 19; 26(2):138-46. PubMed ID: 16470734
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  • 18. Prenatal diagnosis of the distal 11q deletion and review of the literature.
    Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Chen LF, Wang W.
    Prenat Diagn; 2004 Feb 19; 24(2):130-6. PubMed ID: 14974122
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  • 19. A paternal balanced translocation [t(7;22)(q32;q13.3)] leading to reciprocal unbalanced karyotypes in two consecutive pregnancies.
    Zackowski JL, Raffel LJ, McDaniel LD, Schwartz S.
    Ann Genet; 1990 Feb 19; 33(2):113-6. PubMed ID: 2241085
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