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Journal Abstract Search

149 related items for PubMed ID: 20681221

  • 1. Two cases with partial trisomy 9: cytogenetic and clinical findings.
    Ozer O, Derbent M, Sahin FI, Yilmaz Z.
    Genet Couns; 2010; 21(2):205-13. PubMed ID: 20681221
    [Abstract] [Full Text] [Related]

  • 2. 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; 18(1):29-48. PubMed ID: 17515299
    [Abstract] [Full Text] [Related]

  • 3. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R, Paolieri M, Anichini C, Scarinci R, Berardi R, Rosaia L, Pucci L.
    Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
    [Abstract] [Full Text] [Related]

  • 4. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 Apr; 19(2):199-209. PubMed ID: 18618995
    [Abstract] [Full Text] [Related]

  • 5. The phenotypic and cytogenetic spectrum of partial trisomy 9.
    Wilson GN, Raj A, Baker D.
    Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
    [Abstract] [Full Text] [Related]

  • 6. Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases.
    Chantot-Bastaraud S, Muti C, Pipiras E, Routon MC, Roubergue A, Burglen L, Siffroi JP, Simon-Bouy B.
    Ann Genet; 2004 Feb; 47(3):241-9. PubMed ID: 15337469
    [Abstract] [Full Text] [Related]

  • 7. 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 Feb; 21(1):99-108. PubMed ID: 20420036
    [Abstract] [Full Text] [Related]

  • 8. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
    Okten G, Sezer O, Günes S, Küçüködük S, Oğur G.
    Genet Couns; 2009 Feb; 20(4):341-7. PubMed ID: 20162869
    [Abstract] [Full Text] [Related]

  • 9. The trisomy 4p syndrome: case report and review.
    Gonzalez CH, Sommer A, Meisner LF, Elejalde BR, Opitz JM.
    Am J Med Genet; 1977 Feb; 1(2):137-56. PubMed ID: 416713
    [Abstract] [Full Text] [Related]

  • 10. 4p trisomy syndrome: report of 4 additional cases and segregation analysis of 21 families with different translocations.
    Crane J, Sujansky E, Smith A.
    Am J Med Genet; 1979 Feb; 4(3):219-29. PubMed ID: 517577
    [Abstract] [Full Text] [Related]

  • 11. Distal 2q duplication: report of two familial cases and an attempt to define a syndrome.
    Zankl M, Schwanitz G, Schmid P, Zankl H, Dockter G, Rodewald A, Zang KD, Grosse KP.
    Am J Med Genet; 1979 Feb; 4(1):5-16. PubMed ID: 495653
    [Abstract] [Full Text] [Related]

  • 12. Distal partial trisomy 1q: report of two cases and a review of the literature.
    Utine GE, Aktas D, Alanay Y, Gücer S, Tuncbilek E, Mrasek K, Liehr T.
    Prenat Diagn; 2007 Sep; 27(9):865-71. PubMed ID: 17605151
    [Abstract] [Full Text] [Related]

  • 13. Partial duplication of the short arm of chromosome 2 (dup(2)(p13----p21) associated with mental retardation and an Aarskog-like phenotype.
    Fryns JP, Kleczkowska A, Kenis H, Decock P, Van den Berghe H.
    Ann Genet; 1989 Sep; 32(3):174-6. PubMed ID: 2573314
    [Abstract] [Full Text] [Related]

  • 14. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR, Weiss L, Van Dyke DL, Jarvi P.
    Am J Med Genet; 1981 Sep; 10(4):357-65. PubMed ID: 7332029
    [Abstract] [Full Text] [Related]

  • 15. Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.
    Hacihanefioğlu S, Güven GS, Deviren A, Silahtaroğlu AN, Yosunvkaya Fenerci E, Ozkiliç A, Yüksel A.
    Genet Couns; 2002 Sep; 13(1):41-8. PubMed ID: 12017237
    [Abstract] [Full Text] [Related]

  • 16. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
    Liang DS, Wu LQ, Cai F, Xia K, Long ZG, Pan Q, Dai HP, Xia JH.
    Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
    [Abstract] [Full Text] [Related]

  • 17. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
    El-Ruby M, Hemly NA, Zaki MS.
    Genet Couns; 2007 Feb; 18(2):217-26. PubMed ID: 17710874
    [Abstract] [Full Text] [Related]

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  • 19. 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 Feb; 11(4):355-61. PubMed ID: 11140413
    [Abstract] [Full Text] [Related]

  • 20. Cytogenetic and molecular analysis in trisomy 12p.
    Allen TL, Brothman AR, Carey JC, Chance PF.
    Am J Med Genet; 1996 May 03; 63(1):250-6. PubMed ID: 8723118
    [Abstract] [Full Text] [Related]

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