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

159 related items for PubMed ID: 3688018

  • 1. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
    Kousseff BG, Diamond T, Essig Y, Miller K, Tedesco T.
    Am J Med Genet; 1987 Dec; 28(4):803-11. PubMed ID: 3688018
    [Abstract] [Full Text] [Related]

  • 2. The cytogenetic controversy in the Prader-Labhart-Willi syndrome.
    Kousseff BG.
    Am J Med Genet; 1982 Dec; 13(4):431-9. PubMed ID: 7158643
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. [Prader-Labhart-Willi syndrome in infants].
    Schmeling H, Gillessen-Kaesbach G, Schulte-Mattler U, Burdach S, Horneff G.
    Klin Padiatr; 2002 Mar 01; 214(2):51-3. PubMed ID: 11972309
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomy.
    Saitoh S, Hosoki K, Takano K, Tonoki H.
    Clin Genet; 2007 Oct 01; 72(4):378-80. PubMed ID: 17850637
    [No Abstract] [Full Text] [Related]

  • 15. Sister chromatid exchange analysis in the Prader-Labhart-Willi syndrome.
    Butler MG, Jenkins BB.
    Am J Med Genet; 1987 Dec 01; 28(4):821-7. PubMed ID: 3688020
    [Abstract] [Full Text] [Related]

  • 16. 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 01; 28(4):829-38. PubMed ID: 3688021
    [Abstract] [Full Text] [Related]

  • 17. Inv dup(15) supernumerary marker chromosomes.
    Webb T.
    J Med Genet; 1994 Aug 01; 31(8):585-94. PubMed ID: 7815414
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome.
    Butler MG, Jenkins BB.
    Am J Med Genet; 1989 Apr 01; 32(4):514-9. PubMed ID: 2505618
    [Abstract] [Full Text] [Related]

  • 20. A Y/15 translocation in a 45,X male with Prader-Willi syndrome.
    Puvabanditsin S, Garrow E, Razi S, Mohar AG, Tadros JJ, Phattraprayoon N, Patel P.
    Genet Couns; 2007 Apr 01; 18(4):417-21. PubMed ID: 18286823
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.