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272 related items for PubMed ID: 16023554

  • 1. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.
    Battaglia A.
    Brain Dev; 2005 Aug; 27(5):365-9. PubMed ID: 16023554
    [Abstract] [Full Text] [Related]

  • 2. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
    Battaglia A.
    Orphanet J Rare Dis; 2008 Nov 19; 3():30. PubMed ID: 19019226
    [Abstract] [Full Text] [Related]

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

  • 4. Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
    Flejter WL, Bennett-Baker PE, Ghaziuddin M, McDonald M, Sheldon S, Gorski JL.
    Am J Med Genet; 1996 Jan 11; 61(2):182-7. PubMed ID: 8669450
    [Abstract] [Full Text] [Related]

  • 5. Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.
    Hou JW, Wang TR.
    Eur J Pediatr; 1998 Feb 11; 157(2):122-7. PubMed ID: 9504785
    [Abstract] [Full Text] [Related]

  • 6. The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.
    Battaglia A, Gurrieri F, Bertini E, Bellacosa A, Pomponi MG, Paravatou-Petsotas M, Mazza S, Neri G.
    Neurology; 1997 Apr 11; 48(4):1081-6. PubMed ID: 9109904
    [Abstract] [Full Text] [Related]

  • 7. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.
    Blennow E, Nielsen KB, Telenius H, Carter NP, Kristoffersson U, Holmberg E, Gillberg C, Nordenskjöld M.
    Am J Med Genet; 1995 Jan 02; 55(1):85-94. PubMed ID: 7702104
    [Abstract] [Full Text] [Related]

  • 8. Inv dup (15): is the electroclinical phenotype helpful for this challenging clinical diagnosis?
    Valente KD, Freitas A, Fridman C, Varela M, Silva AE, Fett AC, Koiffmann CP.
    Clin Neurophysiol; 2006 Apr 02; 117(4):803-9. PubMed ID: 16495142
    [Abstract] [Full Text] [Related]

  • 9. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
    Chen CP, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2016 Oct 02; 55(5):728-732. PubMed ID: 27751425
    [Abstract] [Full Text] [Related]

  • 10. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
    Mignon-Ravix C, Depetris D, Luciani JJ, Cuoco C, Krajewska-Walasek M, Missirian C, Collignon P, Delobel B, Croquette MF, Moncla A, Kroisel PM, Mattei MG.
    Eur J Hum Genet; 2007 Apr 02; 15(4):432-40. PubMed ID: 17264869
    [Abstract] [Full Text] [Related]

  • 11. Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15.
    Takeda Y, Baba A, Nakamura F, Ito M, Honma H, Koyama T.
    Seizure; 2000 Mar 02; 9(2):145-50. PubMed ID: 10845741
    [Abstract] [Full Text] [Related]

  • 12. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Zuberi SM, Carey JC.
    Pediatrics; 2008 Feb 02; 121(2):404-10. PubMed ID: 18245432
    [Abstract] [Full Text] [Related]

  • 13. Rearrangements of chromosome 15 in epilepsy.
    Torrisi L, Sangiorgi E, Russo L, Gurrieri F.
    Am J Med Genet; 2001 Feb 02; 106(2):125-8. PubMed ID: 11579432
    [Abstract] [Full Text] [Related]

  • 14. Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.
    Huang B, Crolla JA, Christian SL, Wolf-Ledbetter ME, Macha ME, Papenhausen PN, Ledbetter DH.
    Hum Genet; 1997 Jan 02; 99(1):11-7. PubMed ID: 9003485
    [Abstract] [Full Text] [Related]

  • 15. Familial partial trisomy 15q11-13 presenting as intractable epilepsy in the child and schizophrenia in the mother.
    Michelson M, Eden A, Vinkler C, Leshinsky-Silver E, Kremer U, Lerman-Sagie T, Lev D.
    Eur J Paediatr Neurol; 2011 May 02; 15(3):230-3. PubMed ID: 21145272
    [Abstract] [Full Text] [Related]

  • 16. Del 1p36 syndrome: a newly emerging clinical entity.
    Battaglia A.
    Brain Dev; 2005 Aug 02; 27(5):358-61. PubMed ID: 16023552
    [Abstract] [Full Text] [Related]

  • 17. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
    Guo WJ, Callif-Daley F, Zapata MC, Miller ME.
    Am J Med Genet; 1995 Sep 11; 58(3):230-6. PubMed ID: 8533823
    [Abstract] [Full Text] [Related]

  • 18. FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.
    Cockwell AE, Dávalos IP, Rivera HR, Crolla JA.
    Am J Med Genet; 2001 Nov 01; 103(4):289-94. PubMed ID: 11746008
    [Abstract] [Full Text] [Related]

  • 19. Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.
    Kaplan LC, Wharton R, Elias E, Mandell F, Donlon T, Latt SA.
    Am J Med Genet; 1987 Sep 01; 28(1):45-53. PubMed ID: 3674117
    [Abstract] [Full Text] [Related]

  • 20. Mosaic 5p tetrasomy.
    Stanley WS, Powell CM, Devine GC, Ellingham T, Samango-Sprouse CA, Vaught DR, Murphy BA, Rosenbaum KN.
    Am J Med Genet; 1993 Mar 15; 45(6):774-6. PubMed ID: 8456861
    [Abstract] [Full Text] [Related]

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