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130 related items for PubMed ID: 21145272

  • 1. 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; 15(3):230-3. PubMed ID: 21145272
    [Abstract] [Full Text] [Related]

  • 2. 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]

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

  • 4. Neurological features and long-term follow-up in 15q11.2-13.1 duplication.
    Coppola A, Ruosi P, Santulli L, Striano S, Zara F, Striano P, Sisodiya SM.
    Eur J Med Genet; 2013 Nov; 56(11):614-8. PubMed ID: 24075935
    [Abstract] [Full Text] [Related]

  • 5. Epilepsy in patients with angelman syndrome caused by deletion of the chromosome 15q11-13.
    Valente KD, Koiffmann CP, Fridman C, Varella M, Kok F, Andrade JQ, Grossmann RM, Marques-Dias MJ.
    Arch Neurol; 2006 Jan; 63(1):122-8. PubMed ID: 16401744
    [Abstract] [Full Text] [Related]

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

  • 7. 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]

  • 8. Microdeletion of chromosome 15q26.1 in a child with intractable generalized epilepsy.
    Dhamija R, Breningstall G, Wong-Kisiel L, Dolan M, Hirsch B, Wirrell E.
    Pediatr Neurol; 2011 Jul 15; 45(1):60-2. PubMed ID: 21723464
    [Abstract] [Full Text] [Related]

  • 9. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C, Moreno-De-Luca D, Heron D, Bouteiller D, Gennetier A, Delorme R, Chaste P, Siffroi JP, Chantot-Bastaraud S, Benyahia B, Trouillard O, Nygren G, Kopp S, Johansson M, Rastam M, Burglen L, Leguern E, Verloes A, Leboyer M, Brice A, Gillberg C, Betancur C.
    Biol Psychiatry; 2009 Aug 15; 66(4):349-59. PubMed ID: 19278672
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 110(3):227-34. PubMed ID: 11935334
    [Abstract] [Full Text] [Related]

  • 11. A cryptic duplication 22q13.31 to qter leads to a distinct phenotype with mental retardation, microcephaly and mild facial dysmorphism.
    Peeters H, Vermeesch J, Fryns JP.
    Genet Couns; 2008 Mar 15; 19(4):365-71. PubMed ID: 19239079
    [Abstract] [Full Text] [Related]

  • 12. Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome.
    Galván-Manso M, Campistol J, Conill J, Sanmartí FX.
    Epileptic Disord; 2005 Mar 15; 7(1):19-25. PubMed ID: 15741136
    [Abstract] [Full Text] [Related]

  • 13. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
    Wyandt HE, Shim SH, Mark HF, Huang XL, Milunsky JM.
    Exp Mol Pathol; 2006 Jun 15; 80(3):262-6. PubMed ID: 16516886
    [Abstract] [Full Text] [Related]

  • 14. 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 Jun 15; 51(6):547-57. PubMed ID: 18692163
    [Abstract] [Full Text] [Related]

  • 15. Duplication of the 15q11-q13 region: clinical and genetic study of 30 new cases.
    Al Ageeli E, Drunat S, Delanoë C, Perrin L, Baumann C, Capri Y, Fabre-Teste J, Aboura A, Dupont C, Auvin S, El Khattabi L, Chantereau D, Moncla A, Tabet AC, Verloes A.
    Eur J Med Genet; 2014 Jan 15; 57(1):5-14. PubMed ID: 24239951
    [Abstract] [Full Text] [Related]

  • 16. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
    Klein OD, Cotter PD, Albertson DG, Pinkel D, Tidyman WE, Moore MW, Rauen KA.
    Clin Genet; 2004 Jun 15; 65(6):477-82. PubMed ID: 15151506
    [Abstract] [Full Text] [Related]

  • 17. Trisomy of medial 15q as result of an analphoid supernumerary ring chromosome detected by CGH and FISH.
    Constantinou M, Płowás I, Kałuzewski B.
    Cytogenet Genome Res; 2007 Jun 15; 119(1-2):165-9. PubMed ID: 18160798
    [Abstract] [Full Text] [Related]

  • 18. Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.
    Murthy SK, Nygren AO, El Shakankiry HM, Schouten JP, Al Khayat AI, Ridha A, Al Ali MT.
    Cytogenet Genome Res; 2007 Jun 15; 116(1-2):135-40. PubMed ID: 17268193
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 15(4):432-40. PubMed ID: 17264869
    [Abstract] [Full Text] [Related]

  • 20. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
    Engelen JJ, Loots WJ, Albrechts JC, Schrander-Stumpel CT, Dirckx R, Smeets HJ, Hamers AJ, Geraedts JP.
    Genet Couns; 1999 Apr 15; 10(2):123-32. PubMed ID: 10422004
    [Abstract] [Full Text] [Related]

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