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Journal Abstract Search

126 related items for PubMed ID: 9843058

  • 1. Prader-Willi syndrome phenotype in X chromosome anomalies: evidence for a distinct syndrome.
    Stratakis CA.
    Am J Med Genet; 1998 Nov 16; 80(3):294-5, 300-1. PubMed ID: 9843058
    [No Abstract] [Full Text] [Related]

  • 2. [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 16; 37(5):255-61. PubMed ID: 4023109
    [Abstract] [Full Text] [Related]

  • 3. 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 May 16; 10(2):123-32. PubMed ID: 10422004
    [Abstract] [Full Text] [Related]

  • 4. Prader--Willi syndrome associated with an interstitial deletion of chromosome 15.
    Bonuccelli CM, Stetten G, Levitt RC, Levin LS, Pyeritz RE.
    Johns Hopkins Med J; 1982 Nov 16; 151(5):237-42. PubMed ID: 7143875
    [No Abstract] [Full Text] [Related]

  • 5. 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 Nov 16; 49(4):298-305. PubMed ID: 16829351
    [Abstract] [Full Text] [Related]

  • 6. 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 Nov 16; 11(2):119-26. PubMed ID: 10893663
    [Abstract] [Full Text] [Related]

  • 7. PDD and Prader-Willi syndrome.
    Demb HB, Papola P.
    J Am Acad Child Adolesc Psychiatry; 1995 May 16; 34(5):539-40. PubMed ID: 7775350
    [No Abstract] [Full Text] [Related]

  • 8. The cytogenetic controversy regarding the Prader-Willi syndrome.
    Kousseff BG, Douglass R.
    Birth Defects Orig Artic Ser; 1982 May 16; 18(3B):301-4. PubMed ID: 6958334
    [No Abstract] [Full Text] [Related]

  • 9. Kleine-Levin syndrome in a boy with Prader-Willi syndrome.
    Gau SF, Soong WT, Liu HM, Hou JW, Tsai WY, Chiu YN, Yeh YC, Wang PJ, Wang TR.
    Sleep; 1996 Jan 16; 19(1):13-7. PubMed ID: 8650457
    [Abstract] [Full Text] [Related]

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  • 11. Prader-Willi habitus, osteopenia, and camptodactyly (Urban-Rogers-Meyer syndrome): a probable second report.
    Pagnan NA, Gollop TR.
    Am J Med Genet; 1988 Dec 16; 31(4):787-92. PubMed ID: 3239569
    [Abstract] [Full Text] [Related]

  • 12. Recombinant DNA and the analysis of cytogenetic disorders associated with mental retardation.
    Gerald PS, Bruns GA.
    Res Publ Assoc Res Nerv Ment Dis; 1983 Dec 16; 60():173-9. PubMed ID: 6337391
    [No Abstract] [Full Text] [Related]

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  • 14. 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 Dec 16; 18(4):417-21. PubMed ID: 18286823
    [Abstract] [Full Text] [Related]

  • 15. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems.
    D'Angelo CS, Da Paz JA, Kim CA, Bertola DR, Castro CI, Varela MC, Koiffmann CP.
    Eur J Med Genet; 2006 Dec 16; 49(6):451-60. PubMed ID: 16564757
    [Abstract] [Full Text] [Related]

  • 16. The Prader-Willi phenotype of fragile X syndrome.
    Nowicki ST, Tassone F, Ono MY, Ferranti J, Croquette MF, Goodlin-Jones B, Hagerman RJ.
    J Dev Behav Pediatr; 2007 Apr 16; 28(2):133-8. PubMed ID: 17435464
    [Abstract] [Full Text] [Related]

  • 17. 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 16; 72(4):378-80. PubMed ID: 17850637
    [No Abstract] [Full Text] [Related]

  • 18. Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus.
    Kondo I, Hamabe J, Yamamoto K, Niikawa N.
    Clin Genet; 1990 Dec 16; 38(6):422-6. PubMed ID: 1981180
    [Abstract] [Full Text] [Related]

  • 19. The Prader-Willi syndrome and the Angelman syndrome.
    Vogels A, Fryns JP.
    Genet Couns; 2002 Dec 16; 13(4):385-96. PubMed ID: 12558108
    [Abstract] [Full Text] [Related]

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