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Journal Abstract Search

397 related items for PubMed ID: 9504785

  • 1. 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; 157(2):122-7. PubMed ID: 9504785
    [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. 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 19; 35(5):425-8. PubMed ID: 9610809
    [Abstract] [Full Text] [Related]

  • 4. 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 19; 55(5):728-732. PubMed ID: 27751425
    [Abstract] [Full Text] [Related]

  • 5. 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 Oct 19; 3(1):49-55. PubMed ID: 7767656
    [Abstract] [Full Text] [Related]

  • 6. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
    Spinner NB, Zackai E, Cheng SD, Knoll JH.
    Am J Med Genet; 1995 May 22; 57(1):61-5. PubMed ID: 7645601
    [Abstract] [Full Text] [Related]

  • 7. 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 22; 55(4):753-9. PubMed ID: 7942854
    [Abstract] [Full Text] [Related]

  • 8. 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 22; 99(1):11-7. PubMed ID: 9003485
    [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 Jan 22; 1(1):37-50. PubMed ID: 8069650
    [Abstract] [Full Text] [Related]

  • 10. 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 22; 48(4):1081-6. PubMed ID: 9109904
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes.
    Webb T, Hardy CA, King M, Watkiss E, Mitchell C, Cole T.
    Clin Genet; 1998 Jan 02; 53(1):34-43. PubMed ID: 9550359
    [Abstract] [Full Text] [Related]

  • 13. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.
    Battaglia A.
    Brain Dev; 2005 Aug 02; 27(5):365-9. PubMed ID: 16023554
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
    Robinson WP, Wagstaff J, Bernasconi F, Baccichetti C, Artifoni L, Franzoni E, Suslak L, Shih LY, Aviv H, Schinzel AA.
    J Med Genet; 1993 Sep 11; 30(9):756-60. PubMed ID: 8411071
    [Abstract] [Full Text] [Related]

  • 16. Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.
    Ungaro P, Christian SL, Fantes JA, Mutirangura A, Black S, Reynolds J, Malcolm S, Dobyns WB, Ledbetter DH.
    J Med Genet; 2001 Jan 11; 38(1):26-34. PubMed ID: 11134237
    [Abstract] [Full Text] [Related]

  • 17. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
    Leana-Cox J, Jenkins L, Palmer CG, Plattner R, Sheppard L, Flejter WL, Zackowski J, Tsien F, Schwartz S.
    Am J Hum Genet; 1994 May 11; 54(5):748-56. PubMed ID: 8178816
    [Abstract] [Full Text] [Related]

  • 18. Inv dup(15) supernumerary marker chromosomes.
    Webb T.
    J Med Genet; 1994 Aug 11; 31(8):585-94. PubMed ID: 7815414
    [No Abstract] [Full Text] [Related]

  • 19. 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 11; 43(9):1096-100. PubMed ID: 12199736
    [Abstract] [Full Text] [Related]

  • 20. 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]

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