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Journal Abstract Search

270 related items for PubMed ID: 10687166

  • 41. 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; 28(2):133-8. PubMed ID: 17435464
    [Abstract] [Full Text] [Related]

  • 42. Food as a motivator in a client with Prader Willi syndrome.
    Gault J.
    Nurs Times; 2007 Apr; 92(41):38-9. PubMed ID: 8932152
    [Abstract] [Full Text] [Related]

  • 43. Monozygotic twins concordant for Prader-Willi syndrome.
    Ikeda K, Asaka A, Inouye E, Kaihara H, Kinoshita K.
    Jinrui Idengaku Zasshi; 1973 Sep; 18(2):220-5. PubMed ID: 4797433
    [No Abstract] [Full Text] [Related]

  • 44. [Prader-Willi syndrome--obesity with a genetic background].
    Ritzén M.
    Lakartidningen; 1987 Apr 08; 84(15):1271-3. PubMed ID: 3586782
    [No Abstract] [Full Text] [Related]

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  • 48. Preventing mental retardation associated with gross obesity in the Prader-Willi syndrome.
    Crnic KA, Sulzbacher S, Snow J, Holm VA.
    Pediatrics; 1980 Nov 08; 66(5):787-9. PubMed ID: 7432886
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  • 49. [To know more about the Prader-Willi syndrome. Diagnosis].
    Midro AT, Olchowik B, Lebiedzińska A, Midro H.
    Psychiatr Pol; 2009 Nov 08; 43(2):135-49. PubMed ID: 19697784
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  • 52. 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 08; 34(4):881-6. PubMed ID: 15115105
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  • 53. [A case of Prader-Willi syndrome].
    Hsiao SY, Fukao T, Koro M, Funakoshi Y, Hieda T.
    Shoni Shikagaku Zasshi; 1989 Dec 08; 27(3):700-7. PubMed ID: 2489883
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  • 54. Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.
    Murthy SK, Nygren AO, El Shakankiry HM, Schouten JP, Al Khayat AI, Ridha A, Al Ali MT.
    Cytogenet Genome Res; 2007 Dec 08; 116(1-2):135-40. PubMed ID: 17268193
    [Abstract] [Full Text] [Related]

  • 55. The genetics, diagnosis, and management of Prader-Willi syndrome.
    Nativio DG.
    J Pediatr Health Care; 2002 Dec 08; 16(6):298-303. PubMed ID: 12436099
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  • 56. [Behavioural phenotypes in Prader-Willi syndrome].
    Rosell-Raga L.
    Rev Neurol; 2003 Feb 08; 36 Suppl 1():S153-7. PubMed ID: 12599118
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  • 58. Prevalence of Prader-Willi and Angelman syndromes among mentally retarded boys in Brazil.
    Vercesi AM, Carvalho MR, Aguiar MJ, Pena SD.
    J Med Genet; 1999 Jun 08; 36(6):498. PubMed ID: 10874644
    [No Abstract] [Full Text] [Related]

  • 59. [Prader-Willi syndrome].
    Kousholt AM, Lund HT.
    Ugeskr Laeger; 1982 May 10; 144(19):1394-5. PubMed ID: 7135526
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  • 60. Prader-Willi syndrome: report of a case with special emphasis on oral problems.
    Bazopoulou-Kyrkanidou E, Papagiannoulis L.
    J Clin Pediatr Dent; 1992 May 10; 17(1):37-40. PubMed ID: 1290759
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