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Journal Abstract Search

531 related items for PubMed ID: 7856662

  • 1.
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  • 2. De novo complex chromosome rearrangement: a study of two patients.
    Melo DG, Huber J, Giuliani LR, Mazzucatto LF, Riegel M, Pina-Neto JM.
    Genet Couns; 2004; 15(3):303-10. PubMed ID: 15517822
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  • 4. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
    Karmous-Benailly H, Giuliano F, Massol C, Bloch C, De Ricaud D, Lambert JC, Perelman S.
    Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
    [Abstract] [Full Text] [Related]

  • 5. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
    Wang H, McLaughlin M, Thompson C, Hunter AG.
    Am J Med Genet; 1993 Jun 15; 46(5):559-62. PubMed ID: 8322821
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  • 6. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
    Caliskan MO, Karauzum SB, Mihci E, Tacoy S, Luleci G.
    Genet Couns; 2005 Jun 15; 16(2):129-38. PubMed ID: 16080292
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  • 7. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
    Lukusa T, van den Berghe L, Smeets E, Fryns JP.
    Ann Genet; 1999 Jun 15; 42(4):215-20. PubMed ID: 10674161
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  • 8. Recombinant balanced and unbalanced translocations as a consequence of a balanced complex chromosomal rearrangement involving eight breakpoints in four chromosomes.
    Röthlisberger B, Kotzot D, Brecevic L, Koehler M, Balmer D, Binkert F, Schinzel A.
    Eur J Hum Genet; 1999 Dec 15; 7(8):873-83. PubMed ID: 10602362
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  • 9. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report.
    Mundhofir FE, Kooper AJ, Winarni TI, Smits AP, Faradz SM, Hamel BC.
    Genet Couns; 2010 Dec 15; 21(1):99-108. PubMed ID: 20420036
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  • 10. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
    Fryns JP, Kleczkowska A, Kenis H.
    Ann Genet; 1984 Dec 15; 27(1):62-4. PubMed ID: 6609678
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  • 12. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
    Giardino D, Corti C, Ballarati L, Finelli P, Valtorta C, Botta G, Giudici M, Grosso E, Larizza L.
    Prenat Diagn; 2006 Jun 15; 26(6):565-70. PubMed ID: 16683274
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  • 13. De novo apparently balanced complex chromosome rearrangement (CCR) involving chromosomes 4, 18, and 21 in a girl with mental retardation: report and review.
    Batanian JR, Eswara MS.
    Am J Med Genet; 1998 Jun 16; 78(1):44-51. PubMed ID: 9637422
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  • 14. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
    Esmer MC, Carnevale A, Gómez L, del Castillo V, Frías S.
    Rev Invest Clin; 1996 Jun 16; 48(1):27-33. PubMed ID: 8815483
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  • 15. Reproductive risks for carriers of complex chromosome rearrangements: analysis of 25 families.
    Gorski JL, Kistenmacher ML, Punnett HH, Zackai EH, Emanuel BS.
    Am J Med Genet; 1988 Feb 16; 29(2):247-61. PubMed ID: 3354596
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  • 16. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
    Schürmann M, Wethling H, Niemeyer ML, Schwinger E.
    Klin Padiatr; 1987 Feb 16; 199(1):27-31. PubMed ID: 2435950
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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 16; 26(2):138-46. PubMed ID: 16470734
    [Abstract] [Full Text] [Related]

  • 18. Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features.
    Kleefstra T, van de Zande G, Merkx G, Mieloo H, Hoovers JM, Smeets D.
    Eur J Hum Genet; 2000 Aug 16; 8(8):637-40. PubMed ID: 10951526
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  • 19. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.
    Zackai EH, Emanuel BS.
    Am J Med Genet; 1980 Aug 16; 7(4):507-21. PubMed ID: 7211960
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  • 20. 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
    [Abstract] [Full Text] [Related]

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