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

475 related items for PubMed ID: 18618997

  • 21. Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking.
    Liu S, Zhang K, Song F, Yang Y, Lv Y, Gao M, Liu Y, Gai Z.
    Cytogenet Genome Res; 2017; 152(1):1-8. PubMed ID: 28647735
    [Abstract] [Full Text] [Related]

  • 22. Mosaic maternal uniparental disomy of chromosome 15 in Prader-Willi syndrome: utility of genome-wide SNP array.
    Izumi K, Santani AB, Deardorff MA, Feret HA, Tischler T, Thiel BD, Mulchandani S, Stolle CA, Spinner NB, Zackai EH, Conlin LK.
    Am J Med Genet A; 2013 Jan; 161A(1):166-71. PubMed ID: 23225330
    [Abstract] [Full Text] [Related]

  • 23. 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; 65(6):477-82. PubMed ID: 15151506
    [Abstract] [Full Text] [Related]

  • 24. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.
    Gregory CA, Kirkilionis AJ, Greenberg CR, Chudley AE, Hamerton JL.
    Am J Med Genet; 1990 Apr; 35(4):536-45. PubMed ID: 1970703
    [Abstract] [Full Text] [Related]

  • 25. 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]

  • 26. A case described as translocation 15;15 revised: maternal 15 UPD, resulting from isochromosome 15, in a PWS patient.
    Gutkowska A, Tylki-Szymańska A, Popowska E, Bielińska B, Jurkiewicz D, Krajewska-Walasek M.
    Eur J Med Genet; 2005 Aug 15; 48(2):207-9. PubMed ID: 16053914
    [No Abstract] [Full Text] [Related]

  • 27. A variety of genetic mechanisms are associated with the Prader-Willi syndrome.
    Woodage T, Deng ZM, Prasad M, Smart R, Lindeman R, Christian SL, Ledbetter DH, Robson L, Smith A, Trent RJ.
    Am J Med Genet; 1994 Sep 15; 54(3):219-26. PubMed ID: 7810579
    [Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. Segmental maternal heterodisomy of the proximal part of chromosome 15 in an infant with Prader-Willi syndrome.
    Nazarenko S, Sazhenova E, Baumer A, Schinzel A.
    Eur J Hum Genet; 2004 May 15; 12(5):411-4. PubMed ID: 14997184
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
    Camprubí C, Coll MD, Villatoro S, Gabau E, Kamli A, Martínez MJ, Poyatos D, Guitart M.
    Eur J Med Genet; 2007 May 15; 50(1):11-20. PubMed ID: 17095305
    [Abstract] [Full Text] [Related]

  • 34. A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array.
    Morandi A, Bonnefond A, Lobbens S, Carotenuto M, Del Giudice EM, Froguel P, Maffeis C.
    Am J Med Genet A; 2015 Nov 15; 167A(11):2720-6. PubMed ID: 26109092
    [Abstract] [Full Text] [Related]

  • 35. Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.
    Mitchell J, Schinzel A, Langlois S, Gillessen-Kaesbach G, Schuffenhauer S, Michaelis R, Abeliovich D, Lerer I, Christian S, Guitart M, McFadden DE, Robinson WP.
    Am J Med Genet; 1996 Oct 16; 65(2):133-6. PubMed ID: 8911605
    [Abstract] [Full Text] [Related]

  • 36. Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?
    Kim HJ, Cho HJ, Jin DK, Kwon EK, Ki CS, Kim JW, Kim SH.
    Clin Genet; 2004 Oct 16; 66(4):368-72. PubMed ID: 15355442
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. A combination of five short tandem repeats of chromosome 15 significantly improves the identification of Prader-Willi syndrome etiology in the Argentinean population.
    Aráoz HV, Torrado M, Barreiro C, Chertkoff L.
    Genet Mol Res; 2006 Jun 30; 5(2):390-8. PubMed ID: 16819717
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. 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]

    Page: [Previous] [Next] [New Search]
    of 24.