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Journal Abstract Search

270 related items for PubMed ID: 10687166

  • 1. [Report of case of Prader-Willi syndrome].
    Visco G, Ughi M, Trevenzoli G.
    Pediatr Med Chir; 1999; 21(3):149-50. PubMed ID: 10687166
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  • 4. [Prader-Willi syndrome or Angelman syndrome? A question of maternal or paternal chromosome 15].
    Ritzén M, Anvret M.
    Lakartidningen; 1992 May 27; 89(22):1985-6. PubMed ID: 1630213
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  • 9. [Diagnosis of Prader-Willi syndrome. Considerations on a case of erroneous diagnosis].
    Scommegna S, Zollino M, Paolone G.
    Pediatr Med Chir; 2001 May 27; 23(3-4):191-6. PubMed ID: 11723857
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  • 11. 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 May 27; 11(2):119-26. PubMed ID: 10893663
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  • 12. 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 May 27; 49(4):298-305. PubMed ID: 16829351
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  • 14. [Prader-Labhart-Willi syndrome in infants].
    Schmeling H, Gillessen-Kaesbach G, Schulte-Mattler U, Burdach S, Horneff G.
    Klin Padiatr; 2002 May 27; 214(2):51-3. PubMed ID: 11972309
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  • 16. Neonatal presentation of Prader Willi sindrome. Personal records.
    Maggio MC, Corsello M, Piccione M, Piro E, Giuffrè M, Liotta A.
    Minerva Pediatr; 2007 Dec 27; 59(6):817-23. PubMed ID: 17978792
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  • 20. 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 27; 66(4):368-72. PubMed ID: 15355442
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