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

345 related items for PubMed ID: 19019226

  • 1. 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]

  • 2. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.
    Battaglia A.
    Brain Dev; 2005 Aug 19; 27(5):365-9. PubMed ID: 16023554
    [Abstract] [Full Text] [Related]

  • 3. 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 19; 157(2):122-7. PubMed ID: 9504785
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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 15; 55(5):728-732. PubMed ID: 27751425
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 99(1):11-7. PubMed ID: 9003485
    [Abstract] [Full Text] [Related]

  • 7. Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes.
    Abeliovich D, Dagan J, Werner M, Lerer I, Shapira Y, Meiner V.
    Eur J Hum Genet; 1995 Jan 15; 3(1):49-55. PubMed ID: 7767656
    [Abstract] [Full Text] [Related]

  • 8. 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 15; 48(4):1081-6. PubMed ID: 9109904
    [Abstract] [Full Text] [Related]

  • 9. Clinical and molecular analysis of five inv dup(15) patients.
    Robinson WP, Binkert F, Giné R, Vazquez C, Müller W, Rosenkranz W, Schinzel A.
    Eur J Hum Genet; 1993 Apr 15; 1(1):37-50. PubMed ID: 8069650
    [Abstract] [Full Text] [Related]

  • 10. Maternal uniparental disomy in a patient with Prader-Willi syndrome with an additional small inv dup(15) chromosome.
    Wang YM, Chuang L, Wang BT, Kuo PL.
    J Formos Med Assoc; 2004 Dec 15; 103(12):943-7. PubMed ID: 15624046
    [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 15; 9(2):145-50. PubMed ID: 10845741
    [Abstract] [Full Text] [Related]

  • 12. Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.
    Cheng SD, Spinner NB, Zackai EH, Knoll JH.
    Am J Hum Genet; 1994 Oct 15; 55(4):753-9. PubMed ID: 7942854
    [Abstract] [Full Text] [Related]

  • 13. Partial hexasomy of chromosome 15.
    Huang B, Bartley J.
    Am J Med Genet A; 2003 Sep 01; 121A(3):277-80. PubMed ID: 12923871
    [Abstract] [Full Text] [Related]

  • 14. Spectrum of epilepsy and electroencephalogram patterns in idic (15) syndrome.
    Battaglia A, Bernardini L, Torrente I, Novelli A, Scarselli G.
    Am J Med Genet A; 2016 Oct 01; 170(10):2531-9. PubMed ID: 27513709
    [Abstract] [Full Text] [Related]

  • 15. Mild generalized epilepsy and developmental disorder associated with large inv dup(15).
    Chifari R, Guerrini R, Pierluigi M, Cavani S, Sgrò V, Elia M, Canger R, Canevini MP.
    Epilepsia; 2002 Sep 01; 43(9):1096-100. PubMed ID: 12199736
    [Abstract] [Full Text] [Related]

  • 16. Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.
    Long FL, Duckett DP, Billam LJ, Williams DK, Crolla JA.
    J Med Genet; 1998 May 01; 35(5):425-8. PubMed ID: 9610809
    [Abstract] [Full Text] [Related]

  • 17. The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings.
    Buoni S, Sorrentino L, Farnetani MA, Pucci L, Fois A.
    J Child Neurol; 2000 Jun 01; 15(6):380-5. PubMed ID: 10868780
    [Abstract] [Full Text] [Related]

  • 18. A study of two Chinese patients with tetrasomy and pentasomy 15q11q13 including Prader-Willi/Angelman syndrome critical region present with developmental delays and mental impairment.
    Yang J, Yang Y, Huang Y, Hu Y, Chen X, Sun H, Lv Z, Cheng Q, Bao L.
    BMC Med Genet; 2013 Jan 15; 14():9. PubMed ID: 23320815
    [Abstract] [Full Text] [Related]

  • 19. Inv dup(15) supernumerary marker chromosomes.
    Webb T.
    J Med Genet; 1994 Aug 15; 31(8):585-94. PubMed ID: 7815414
    [No Abstract] [Full Text] [Related]

  • 20. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature.
    Li H, Du J, Li W, Cheng D, He W, Yi D, Xiong B, Yuan S, Tu C, Meng L, Luo A, Lin G, Lu G, Tan YQ.
    Mol Cytogenet; 2018 Aug 15; 11():15. PubMed ID: 29441129
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 18.