These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

121 related items for PubMed ID: 26349185

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42. Neuropsychological and behavioural phenotype of Dandy-Walker variant presenting in chromosome 22 trisomy: a case study.
    Searson R, Hare DJ, Sridharan S.
    J Intellect Disabil; 2013 Jun; 17(2):102-6. PubMed ID: 23479418
    [Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 46. Multiple congenital malformations including severe eye anomalies and abnormal cerebellar development with Dandy-Walker malformation in a girl with partial trisomy 3q.
    de Azevedo Moreira LM, Neri FB, de Quadros Uzeda S, de Carvalho AF, Santana GC, Souza FR, Rollemberg JC.
    Ophthalmic Genet; 2005 Mar; 26(1):37-43. PubMed ID: 15823924
    [Abstract] [Full Text] [Related]

  • 47. Partial trisomy 14q due to maternal t(4;14)(p16;q32) in a dysmorphic newborn.
    Dundar M, Uzak A, Saatci C, Akalin H.
    Genet Couns; 2011 Mar; 22(3):287-92. PubMed ID: 22029170
    [Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49. 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 Mar; 17(1):57-63. PubMed ID: 16719278
    [Abstract] [Full Text] [Related]

  • 50. Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
    Melo JB, Matoso E, Polityko A, Saraiva J, Backx L, Vermeesch JR, Kosyakova N, Ewers E, Liehr T, Carreira IM.
    Cytogenet Genome Res; 2009 Mar; 125(2):109-14. PubMed ID: 19729913
    [Abstract] [Full Text] [Related]

  • 51. Interstitial deletion of chromosome 2q associated with ovarian dysgenesis.
    Davis E, Grafe M, Cunniff C, Jones KL, Bogart M.
    Clin Genet; 1991 May; 39(5):386-90. PubMed ID: 1860256
    [Abstract] [Full Text] [Related]

  • 52. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
    Ergun MA, Balci S, Konaç E, Kan D, Menevşe S, Bartsch O.
    Turk J Pediatr; 2004 May; 46(4):384-7. PubMed ID: 15641279
    [Abstract] [Full Text] [Related]

  • 53. An unusual presentation of trisomy 9p syndrome with a partial Dandy-Walker malformation.
    Hannam S, Greenough A, Dawson JM.
    Eur J Pediatr; 1999 Dec; 158(12):1012. PubMed ID: 10592087
    [No Abstract] [Full Text] [Related]

  • 54. Dandy-Walker syndrome and chromosomal abnormalities.
    Imataka G, Yamanouchi H, Arisaka O.
    Congenit Anom (Kyoto); 2007 Dec; 47(4):113-8. PubMed ID: 17988252
    [Abstract] [Full Text] [Related]

  • 55. Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13).
    Cetin Z, Mihci E, Keser I, Luleci G.
    Genet Couns; 2012 Dec; 23(2):207-14. PubMed ID: 22876579
    [Abstract] [Full Text] [Related]

  • 56. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].
    Xiao B, Zhang JM, Ji X, Jiang WT, Hu J, Tao J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):247-50. PubMed ID: 21644216
    [Abstract] [Full Text] [Related]

  • 57. A New Case of a Complex Small Supernumerary Marker Chromosome: A Der(9)t(7;9)(p22;q22) due to a Maternal Balanced Rearrangement.
    Manvelyan M, Simonyan I, Hovhannisyan G, Aroutiounian R, Hamid AB, Liehr T.
    J Pediatr Genet; 2015 Dec; 4(4):199-200. PubMed ID: 27617132
    [Abstract] [Full Text] [Related]

  • 58. Partial trisomy 3p and partial monosomy 11q associated with double outlet right ventricle and septum pellucidum et vergae: a case report.
    Say B, Guzoglu N, Uras N, Candemir Z, Akin I, Dilmen U.
    Genet Couns; 2013 Dec; 24(4):387-91. PubMed ID: 24551981
    [Abstract] [Full Text] [Related]

  • 59. [Systematic genetic analysis for a case with duplication 9p].
    Zhang J, Li H, Jiang S, Li H, Zhang Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):237-9. PubMed ID: 25863095
    [Abstract] [Full Text] [Related]

  • 60. New report of two patients with mosaic trisomy 9 presenting unusual features and longer survival.
    Zen PR, Rosa RF, Rosa RC, Graziadio C, Paskulin GA.
    Sao Paulo Med J; 2011 Dec; 129(6):428-32. PubMed ID: 22249800
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.