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Journal Abstract Search

289 related items for PubMed ID: 12017237

  • 1. 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; 13(1):41-8. PubMed ID: 12017237
    [Abstract] [Full Text] [Related]

  • 2. Joubert syndrome co-existing with partial Xp trisomy: review of the literature.
    Güven GS, Fenerci EY, Deviren A, Ozkiliç A, Yüksel A, Hacihanefioğlu S.
    Genet Couns; 2004; 15(3):321-8. PubMed ID: 15517825
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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; 21(1):99-108. PubMed ID: 20420036
    [Abstract] [Full Text] [Related]

  • 5. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M, Przełozna B, Płodzien M, Bugno M, Wnuk M, Kotylak Z, Słota E.
    J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [A case of partial trisomy 9pter --> q13 due to paternal balanced translocation t (9;21) (q13;q21)].
    Woo KS, Kim KE, Kwon EY, Kim JP, Han JY.
    Korean J Lab Med; 2008 Apr; 28(2):155-9. PubMed ID: 18458513
    [Abstract] [Full Text] [Related]

  • 8. Partial trisomy 4q and monosomy 9p resulting from a familial translocation t(4;9)(q27;p24) in a child with choanal atresia.
    Wouters CH, van Bodegom TM, Moll HA, Govaerts LC.
    Ann Genet; 1999 Apr; 42(3):160-5. PubMed ID: 10526659
    [Abstract] [Full Text] [Related]

  • 9. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
    Rao VV, Carpenter NJ, Gucsavas M, Coldwell J, Say B.
    Am J Med Genet; 1995 Jul 31; 58(1):50-3. PubMed ID: 7573156
    [Abstract] [Full Text] [Related]

  • 10. Malformation syndrome of duplication 12q24.1 leads to qter.
    Melnyk AR, Weiss L, Van Dyke DL, Jarvi P.
    Am J Med Genet; 1981 Jul 31; 10(4):357-65. PubMed ID: 7332029
    [Abstract] [Full Text] [Related]

  • 11. Translocation/duplication of 9p onto a duplicated 4q.
    Rivera H, Figuera LE, Vasquez AI.
    Genet Couns; 1992 Jul 31; 3(4):201-3. PubMed ID: 1472355
    [Abstract] [Full Text] [Related]

  • 12. Abnormal chromosome 9 in a neonate program. Report of three cases.
    Nakamura Y, Sato E, Sakai K, Sakuma S, Hashimoto T, Sindou S.
    Arch Pathol Lab Med; 1990 Feb 31; 114(2):185-7. PubMed ID: 2302035
    [Abstract] [Full Text] [Related]

  • 13. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
    Brambila-Tapia AJ, Neira VA, Vásquez-Velásquez AI, Jimenez-Arredondo RE, Chávez-González EL, Picos-Cárdenas VJ, Fletes-Rayas AL, Figuera LE.
    Genet Couns; 2014 Feb 31; 25(3):289-97. PubMed ID: 25365851
    [Abstract] [Full Text] [Related]

  • 14. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
    Canún S, Mutchinick O, Shaffer LG, Fernández C.
    Am J Med Genet; 1998 Nov 16; 80(3):199-203. PubMed ID: 9843037
    [Abstract] [Full Text] [Related]

  • 15. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
    Akbas E, Polat S, Karakas-Celik S, Altintas ZM, Yildirim M, Yilgor E.
    Genet Couns; 2011 Nov 16; 22(4):417-23. PubMed ID: 22303803
    [Abstract] [Full Text] [Related]

  • 16. Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
    Cantu JM, Salamanca F, Buentello L, Carnevale A, Armendares S.
    Ann Genet; 1975 Mar 16; 18(1):5-11. PubMed ID: 1080038
    [Abstract] [Full Text] [Related]

  • 17. Two cases with partial trisomy 9: cytogenetic and clinical findings.
    Ozer O, Derbent M, Sahin FI, Yilmaz Z.
    Genet Couns; 2010 Mar 16; 21(2):205-13. PubMed ID: 20681221
    [Abstract] [Full Text] [Related]

  • 18. [Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].
    Wang XR, Luo RL, Dai XH, Liu JY.
    Yi Chuan; 2007 Jul 16; 29(7):813-6. PubMed ID: 17646146
    [Abstract] [Full Text] [Related]

  • 19. M-FISH applications in clinical genetics.
    Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G.
    Genet Couns; 2005 Jul 16; 16(3):257-68. PubMed ID: 16259323
    [Abstract] [Full Text] [Related]

  • 20. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
    Littooij AS, Hochstenbach R, Sinke RJ, van Tintelen P, Giltay JC.
    Am J Med Genet; 2002 Apr 22; 109(2):125-32. PubMed ID: 11977161
    [Abstract] [Full Text] [Related]

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