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Journal Abstract Search

223 related items for PubMed ID: 11803514

  • 1.
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  • 2. Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports.
    Simic M, Turk J.
    Eur Child Adolesc Psychiatry; 2004 Dec; 13(6):389-93. PubMed ID: 15619052
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  • 5. The interstitial duplication 15q11.2-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature.
    Urraca N, Cleary J, Brewer V, Pivnick EK, McVicar K, Thibert RL, Schanen NC, Esmer C, Lamport D, Reiter LT.
    Autism Res; 2013 Aug; 6(4):268-79. PubMed ID: 23495136
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  • 6. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
    Roberts SE, Dennis NR, Browne CE, Willatt L, Woods G, Cross I, Jacobs PA, Thomas S.
    Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
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  • 7. A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study.
    Veltman MW, Thompson RJ, Craig EE, Dennis NR, Roberts SE, Moore V, Brown JA, Bolton PF.
    J Autism Dev Disord; 2005 Feb; 35(1):117-27. PubMed ID: 15796127
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  • 8. The genetics of autism.
    Muhle R, Trentacoste SV, Rapin I.
    Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
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  • 9. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
    Koochek M, Harvard C, Hildebrand MJ, Van Allen M, Wingert H, Mickelson E, Holden JJ, Rajcan-Separovic E, Lewis ME.
    Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
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  • 10. Clinical and molecular characterization of a large family with an interstitial 15q11q13 duplication.
    Piard J, Philippe C, Marvier M, Beneteau C, Roth V, Valduga M, Béri M, Bonnet C, Grégoire MJ, Jonveaux P, Leheup B.
    Am J Med Genet A; 2010 Aug; 152A(8):1933-41. PubMed ID: 20635369
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  • 11. Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region.
    Thomas NS, Browne CE, Oley C, Healey S, Crolla JA.
    Hum Genet; 1999 Nov; 105(5):384-7. PubMed ID: 10598802
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  • 12. Brief report: visual-spatial deficit in a 16-year-old girl with maternally derived duplication of proximal 15q.
    Cohen D, Martel C, Wilson A, Déchambre N, Amy C, Duverger L, Guile JM, Pipiras E, Benzacken B, Cavé H, Cohen L, Héron D, Plaza M.
    J Autism Dev Disord; 2007 Sep; 37(8):1585-91. PubMed ID: 17006777
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  • 13. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.
    Cook EH, Lindgren V, Leventhal BL, Courchesne R, Lincoln A, Shulman C, Lord C, Courchesne E.
    Am J Hum Genet; 1997 Apr; 60(4):928-34. PubMed ID: 9106540
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  • 14. Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.
    Repetto GM, White LM, Bader PJ, Johnson D, Knoll JH.
    Am J Med Genet; 1998 Sep 01; 79(2):82-9. PubMed ID: 9741464
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  • 15. A family with a grand-maternally derived interstitial duplication of proximal 15q.
    Boyar FZ, Whitney MM, Lossie AC, Gray BA, Keller KL, Stalker HJ, Zori RT, Geffken G, Mutch J, Edge PJ, Voeller KS, Williams CA, Driscoll DJ.
    Clin Genet; 2001 Dec 01; 60(6):421-30. PubMed ID: 11846734
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  • 16. Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.
    Mohandas TK, Park JP, Spellman RA, Filiano JJ, Mamourian AC, Hawk AB, Belloni DR, Noll WW, Moeschler JB.
    Am J Med Genet; 1999 Feb 12; 82(4):294-300. PubMed ID: 10051161
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  • 17. Routine cytogenetic and FISH studies for 17p11/15q11 duplications and subtelomeric rearrangement studies in children with autism spectrum disorders.
    Keller K, Williams C, Wharton P, Paulk M, Bent-Williams A, Gray B, Ward A, Stalker H, Wallace M, Carter R, Zori R.
    Am J Med Genet A; 2003 Mar 01; 117A(2):105-11. PubMed ID: 12567405
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  • 18. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
    Miller DT, Shen Y, Weiss LA, Korn J, Anselm I, Bridgemohan C, Cox GF, Dickinson H, Gentile J, Harris DJ, Hegde V, Hundley R, Khwaja O, Kothare S, Luedke C, Nasir R, Poduri A, Prasad K, Raffalli P, Reinhard A, Smith SE, Sobeih MM, Soul JS, Stoler J, Takeoka M, Tan WH, Thakuria J, Wolff R, Yusupov R, Gusella JF, Daly MJ, Wu BL.
    J Med Genet; 2009 Apr 01; 46(4):242-8. PubMed ID: 18805830
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  • 19. The behavioral phenotype of the idic(15) syndrome.
    Battaglia A, Parrini B, Tancredi R.
    Am J Med Genet C Semin Med Genet; 2010 Nov 15; 154C(4):448-55. PubMed ID: 20981774
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  • 20. Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: a cytogenetic pitfall.
    Carelle-Calmels N, Girard-Lemaire F, Guérin E, Bieth E, Rudolf G, Biancalana V, Pecheur H, Demil H, Schneider T, de Saint-Martin A, Caron O, Legrain M, Gaston V, Flori E.
    Eur J Med Genet; 2008 Nov 15; 51(6):547-57. PubMed ID: 18692163
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