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Journal Abstract Search

967 related items for PubMed ID: 26022164

  • 1. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
    Kalsner L, Chamberlain SJ.
    Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
    [Abstract] [Full Text] [Related]

  • 2. Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.
    Hogart A, Leung KN, Wang NJ, Wu DJ, Driscoll J, Vallero RO, Schanen NC, LaSalle JM.
    J Med Genet; 2009 Feb; 46(2):86-93. PubMed ID: 18835857
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
    Glenn CC, Driscoll DJ, Yang TP, Nicholls RD.
    Mol Hum Reprod; 1997 Apr 15; 3(4):321-32. PubMed ID: 9237260
    [Abstract] [Full Text] [Related]

  • 5. Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11.
    Thomas NS, Durkie M, Potts G, Sandford R, Van Zyl B, Youings S, Dennis NR, Jacobs PA.
    Eur J Hum Genet; 2006 Jul 15; 14(7):831-7. PubMed ID: 16617304
    [Abstract] [Full Text] [Related]

  • 6. Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.
    Procter M, Chou LS, Tang W, Jama M, Mao R.
    Clin Chem; 2006 Jul 15; 52(7):1276-83. PubMed ID: 16690734
    [Abstract] [Full Text] [Related]

  • 7. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
    Christian SL, Fantes JA, Mewborn SK, Huang B, Ledbetter DH.
    Hum Mol Genet; 1999 Jun 15; 8(6):1025-37. PubMed ID: 10332034
    [Abstract] [Full Text] [Related]

  • 8. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13.
    Hogart A, Wu D, LaSalle JM, Schanen NC.
    Neurobiol Dis; 2010 May 15; 38(2):181-91. PubMed ID: 18840528
    [Abstract] [Full Text] [Related]

  • 9. Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region.
    Mim RA, Soorajkumar A, Kosaji N, Rahman MM, Sarker S, Karuvantevida N, Eshaque TB, Rahaman MA, Islam A, Chowdhury MSJ, Shams N, Uddin KMF, Akter H, Uddin M.
    Brain Behav; 2024 Apr 15; 14(4):e3437. PubMed ID: 38616334
    [Abstract] [Full Text] [Related]

  • 10. [Variation analysis of the number of copies and methylene patterns in region 15q11-q13].
    Laurito S, Roqué M.
    Medicina (B Aires); 2018 Apr 15; 78(1):1-5. PubMed ID: 29360068
    [Abstract] [Full Text] [Related]

  • 11. Mechanisms of imprinting of the Prader-Willi/Angelman region.
    Horsthemke B, Wagstaff J.
    Am J Med Genet A; 2008 Aug 15; 146A(16):2041-52. PubMed ID: 18627066
    [Abstract] [Full Text] [Related]

  • 12. 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 Aug 15; 10(2):123-32. PubMed ID: 10422004
    [Abstract] [Full Text] [Related]

  • 13. Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.
    Aypar U, Brodersen PR, Lundquist PA, Dawson DB, Thorland EC, Hoppman N.
    Am J Med Genet A; 2014 Oct 15; 164A(10):2514-20. PubMed ID: 24975781
    [Abstract] [Full Text] [Related]

  • 14. Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.
    Isles AR, Ingason A, Lowther C, Walters J, Gawlick M, Stöber G, Rees E, Martin J, Little RB, Potter H, Georgieva L, Pizzo L, Ozaki N, Aleksic B, Kushima I, Ikeda M, Iwata N, Levinson DF, Gejman PV, Shi J, Sanders AR, Duan J, Willis J, Sisodiya S, Costain G, Werge TM, Degenhardt F, Giegling I, Rujescu D, Hreidarsson SJ, Saemundsen E, Ahn JW, Ogilvie C, Girirajan SD, Stefansson H, Stefansson K, O'Donovan MC, Owen MJ, Bassett A, Kirov G.
    PLoS Genet; 2016 May 15; 12(5):e1005993. PubMed ID: 27153221
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  • 18. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
    Zeschnigk M, Schmitz B, Dittrich B, Buiting K, Horsthemke B, Doerfler W.
    Hum Mol Genet; 1997 Mar 15; 6(3):387-95. PubMed ID: 9147641
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