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Journal Abstract Search

551 related items for PubMed ID: 20162869

  • 1. 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; 20(4):341-7. PubMed ID: 20162869
    [Abstract] [Full Text] [Related]

  • 2. Molecular and cytogenetic characterization of 9p- abnormalities.
    Teebi AS, Gibson L, McGrath J, Meyn MS, Breg WR, Yang-Feng TL.
    Am J Med Genet; 1993 May 15; 46(3):288-92. PubMed ID: 8488873
    [Abstract] [Full Text] [Related]

  • 3. 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 May 15; 18(1):29-48. PubMed ID: 17515299
    [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 May 15; 19(2):199-209. PubMed ID: 18618995
    [Abstract] [Full Text] [Related]

  • 5. Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
    Chen CP, Lin SP, Lee CC, Town DD, Wang W.
    Genet Couns; 2006 May 15; 17(3):301-6. PubMed ID: 17100198
    [Abstract] [Full Text] [Related]

  • 6. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Chern SR, Lee CC, Chen YJ, Wang W.
    Prenat Diagn; 2005 Dec 15; 25(12):1170-2. PubMed ID: 16315335
    [No Abstract] [Full Text] [Related]

  • 7. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
    Ausems MG, Van Spijker HG, Dijkhuis HJ, Swanenburg De Veye HF, Bijlsma JB.
    Genet Couns; 1996 Dec 15; 7(1):61-5. PubMed ID: 8652090
    [Abstract] [Full Text] [Related]

  • 8. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
    Recalcati MP, Bellini M, Norsa L, Ballarati L, Caselli R, Russo S, Larizza L, Giardino D.
    Gene; 2012 Jul 01; 502(1):40-5. PubMed ID: 22537675
    [Abstract] [Full Text] [Related]

  • 9. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
    Kowalczyk M, Tomaszewska A, Podbioł-Palenta A, Constantinou M, Wawrzkiewicz-Witkowska A, Kowalski J, Kałużewski B, Zajączek S, Srebniak MI.
    Cytogenet Genome Res; 2013 Jul 01; 139(1):9-16. PubMed ID: 22965227
    [Abstract] [Full Text] [Related]

  • 10. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G.
    Prenat Diagn; 2006 Mar 01; 26(3):206-13. PubMed ID: 16450348
    [Abstract] [Full Text] [Related]

  • 11. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
    Brisset S, Joly G, Ozilou C, Lapierre JM, Gosset P, LeLorc'h M, Raoul O, Turleau C, Vekemans M, Romana SP.
    Am J Med Genet; 2002 Dec 15; 113(4):339-45. PubMed ID: 12457405
    [Abstract] [Full Text] [Related]

  • 12. [Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human].
    Karamysheva TV, Matveeva VG, Shorina AP, Rubtsov NB.
    Genetika; 2001 Jun 15; 37(6):811-6. PubMed ID: 11517768
    [Abstract] [Full Text] [Related]

  • 13. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
    Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Huang JK, Lee CC, Wang W.
    Genet Couns; 2006 Jun 15; 17(1):57-63. PubMed ID: 16719278
    [Abstract] [Full Text] [Related]

  • 14. 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 Jun 15; 22(4):417-23. PubMed ID: 22303803
    [Abstract] [Full Text] [Related]

  • 15. Combined trisomy 9P and Shprintzen syndrome resulting from a paternal t(9;22).
    Komatsu H, Kihara A, Komura E, Mitsufuji N, Tsujii H, Kakita S, Ikuta H.
    Genet Couns; 2001 Jun 15; 12(2):137-43. PubMed ID: 11491308
    [Abstract] [Full Text] [Related]

  • 16. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
    Schimmenti LA, Higgins RR, Mendelsohn NJ, Casey TM, Steinberger J, Mammel MC, Wiesner GL.
    Am J Med Genet; 1995 May 22; 57(1):52-6. PubMed ID: 7645598
    [Abstract] [Full Text] [Related]

  • 17. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
    Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP.
    Genet Couns; 1998 May 22; 9(3):215-21. PubMed ID: 9777345
    [Abstract] [Full Text] [Related]

  • 18. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
    Sohn YB, Yun JN, Park SJ, Park MS, Kim SH, Lee JH.
    Ann Clin Lab Sci; 2013 May 22; 43(3):332-6. PubMed ID: 23884231
    [Abstract] [Full Text] [Related]

  • 19. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
    Vásquez-Velásquez AI, García-Castillo HA, González-Mercado MG, Dávalos IP, Raca G, Xu X, Dwyer E, Rivera H.
    Cytogenet Genome Res; 2011 May 22; 132(4):233-8. PubMed ID: 21063078
    [Abstract] [Full Text] [Related]

  • 20. Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies.
    Mihçi E, Ozcan M, Berker-Karaüzüm S, Keser I, Taçoy S, Hapsolat S, Lüleci G.
    Turk J Pediatr; 2009 May 22; 51(5):453-9. PubMed ID: 20112600
    [Abstract] [Full Text] [Related]

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