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

265 related items for PubMed ID: 2646521

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome.
    Qumsiyeh MB, Dalton JD, Gordon PL, Wilroy RS, Tharapel AT.
    Am J Med Genet; 1992 Jan 01; 42(1):109-11. PubMed ID: 1308348
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
    Cassidy SB, Thuline HC, Holm VA.
    Am J Med Genet; 1984 Feb 01; 17(2):485-95. PubMed ID: 6336316
    [Abstract] [Full Text] [Related]

  • 5. A case of Prader Willi syndrome with del 15 (q11-->q13).
    Tunçman G, Tükün A, Yalaz K, Bökesoy I.
    Turk J Pediatr; 1993 Feb 01; 35(4):333-6. PubMed ID: 8160287
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. [Prader-Willi syndrome associated with chromosomal aberration: report of a case].
    Kokura K, Shima H, Mori Y, Ikoma F, Sakamoto H, Furuyama J.
    Hinyokika Kiyo; 1992 Sep 01; 38(9):1079-82. PubMed ID: 1357945
    [Abstract] [Full Text] [Related]

  • 8. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome].
    Witkowski R, Ullrich E, Pietsch P, Weber K, Heller K, Losanowa T, Nitz I.
    Psychiatr Neurol Med Psychol (Leipz); 1985 May 01; 37(5):255-61. PubMed ID: 4023109
    [Abstract] [Full Text] [Related]

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

  • 10. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
    Wiriyaukaradecha S, Patmasiriwat P, Wasant P, Tantiniti P.
    Southeast Asian J Trop Med Public Health; 2003 Dec 01; 34(4):881-6. PubMed ID: 15115105
    [Abstract] [Full Text] [Related]

  • 11. [Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases].
    Pfeiffer RA, Tschech L, Irle U, Wündisch GF.
    Klin Padiatr; 1987 Dec 01; 199(5):329-35. PubMed ID: 3316824
    [Abstract] [Full Text] [Related]

  • 12. A case of an atypically large proximal 15q deletion as cause for Prader-Willi syndrome arising from a de novo unbalanced translocation.
    Hickey SE, Thrush DL, Walters-Sen L, Reshmi SC, Astbury C, Gastier-Foster JM, Atkin J.
    Eur J Med Genet; 2013 Sep 01; 56(9):510-4. PubMed ID: 23856564
    [Abstract] [Full Text] [Related]

  • 13. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.
    Varela MC, Simões-Sato AY, Kim CA, Bertola DR, De Castro CI, Koiffmann CP.
    Eur J Med Genet; 2006 Sep 01; 49(4):298-305. PubMed ID: 16829351
    [Abstract] [Full Text] [Related]

  • 14. Neonatal presentation of Prader Willi sindrome. Personal records.
    Maggio MC, Corsello M, Piccione M, Piro E, Giuffrè M, Liotta A.
    Minerva Pediatr; 2007 Dec 01; 59(6):817-23. PubMed ID: 17978792
    [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. Molecular diagnosis of Prader-Willi syndrome.
    Pangkanon S.
    J Med Assoc Thai; 2003 Aug 01; 86 Suppl 3():S510-6. PubMed ID: 14700141
    [Abstract] [Full Text] [Related]

  • 17. Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence.
    Lukusa T, Fryns JP.
    Genet Couns; 2000 Aug 01; 11(2):119-26. PubMed ID: 10893663
    [Abstract] [Full Text] [Related]

  • 18. [Cytogenetic detection of Prader-Willi syndrome in infancy].
    Götz J, Krüger G, Westphal BC, Pelz L.
    Kinderarztl Prax; 1989 May 01; 57(5):239-43. PubMed ID: 2747122
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13.
    Orstavik KH, Tangsrud SE, Kiil R, Hansteen IL, Steen-Johnsen J, Cassidy SB, Martony A, Anvret M, Tommerup N, Bröndum-Nielsen K.
    Am J Med Genet; 1992 Nov 01; 44(4):534-8. PubMed ID: 1442901
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.