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127 related items for PubMed ID: 20981774

  • 1. 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]

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

  • 3. 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]

  • 4. 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]

  • 5. 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 15; 121(2):404-10. PubMed ID: 18245432
    [Abstract] [Full Text] [Related]

  • 6. Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome.
    Kurosawa K, Kawame H, Okamoto N, Ochiai Y, Akatsuka A, Kobayashi M, Shimohira M, Mizuno S, Wada K, Fukushima Y, Kawawaki H, Yamamoto T, Masuno M, Imaizumi K, Kuroki Y.
    Brain Dev; 2005 Aug 15; 27(5):378-82. PubMed ID: 16023556
    [Abstract] [Full Text] [Related]

  • 7. Cognitive-behavioral features of Wolf-Hirschhorn syndrome and other subtelomeric microdeletions.
    Fisch GS, Grossfeld P, Falk R, Battaglia A, Youngblom J, Simensen R.
    Am J Med Genet C Semin Med Genet; 2010 Nov 15; 154C(4):417-26. PubMed ID: 20981770
    [Abstract] [Full Text] [Related]

  • 8. 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; 15(3):230-3. PubMed ID: 21145272
    [Abstract] [Full Text] [Related]

  • 9. Is Angelman syndrome an alternate result of del(15)(q11q13)?
    Magenis RE, Brown MG, Lacy DA, Budden S, LaFranchi S.
    Am J Med Genet; 1987 Dec 15; 28(4):829-38. PubMed ID: 3688021
    [Abstract] [Full Text] [Related]

  • 10. Unique karyotypes in two patients with Prader-Willi syndrome.
    Narahara K, Hiramoto K, Murakami M, Miyake S, Tsuji K, Yokoyama Y, Namba H, Ninomiya S, Murakami R, Seino Y.
    Am J Med Genet; 1992 Mar 01; 42(5):671-7. PubMed ID: 1632436
    [Abstract] [Full Text] [Related]

  • 11. Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons.
    Williams CA, Gray BA, Hendrickson JE, Stone JW, Cantú ES.
    Am J Med Genet; 1989 Mar 01; 32(3):339-45. PubMed ID: 2786338
    [Abstract] [Full Text] [Related]

  • 12. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
    Magenis RE, Toth-Fejel S, Allen LJ, Black M, Brown MG, Budden S, Cohen R, Friedman JM, Kalousek D, Zonana J.
    Am J Med Genet; 1990 Mar 01; 35(3):333-49. PubMed ID: 2309780
    [Abstract] [Full Text] [Related]

  • 13. Duplication of proximal 15q as a cause of Prader-Willi syndrome.
    Pettigrew AL, Gollin SM, Greenberg F, Riccardi VM, Ledbetter DH.
    Am J Med Genet; 1987 Dec 01; 28(4):791-802. PubMed ID: 3688017
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 157(2):122-7. PubMed ID: 9504785
    [Abstract] [Full Text] [Related]

  • 15. Deletions of proximal 15q without Prader-Willi syndrome.
    Greenberg F, Ledbetter DH.
    Am J Med Genet; 1987 Dec 01; 28(4):813-20. PubMed ID: 3688019
    [Abstract] [Full Text] [Related]

  • 16. 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 Dec 01; 11():15. PubMed ID: 29441129
    [Abstract] [Full Text] [Related]

  • 17. Autism in Angelman syndrome: an exploration of comorbidity.
    Trillingsgaard A, ØStergaard JR.
    Autism; 2004 Jun 01; 8(2):163-74. PubMed ID: 15165432
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 117(4):803-9. PubMed ID: 16495142
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 57(1):5-14. PubMed ID: 24239951
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 48(4):1081-6. PubMed ID: 9109904
    [Abstract] [Full Text] [Related]

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