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Journal Abstract Search

267 related items for PubMed ID: 9690933

  • 1. Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome.
    van Lieshout CF, De Meyer RE, Curfs LM, Fryns JP.
    J Child Psychol Psychiatry; 1998 Jul; 39(5):699-710. PubMed ID: 9690933
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  • 3. Personality profiles of youngsters with velo-cardio-facial syndrome.
    Prinzie P, Swillen A, Vogels A, Kockuyt V, Curfs L, Haselager G, Hellinckx W, Devriendt K, Onghena P, Van Lieshout CF, Fryns JP.
    Genet Couns; 2002 Jul; 13(3):265-80. PubMed ID: 12416634
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  • 6. Refining behavioral phenotypes: personality-motivation in Williams and Prader-Willi syndromes.
    Dykens EM, Rosner BA.
    Am J Ment Retard; 1999 Mar; 104(2):158-69. PubMed ID: 10207579
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  • 9. Behavioral phenotypes in genetic syndromes: genetic clues to human behavior.
    Cassidy SB, Morris CA.
    Adv Pediatr; 2002 Mar; 49():59-86. PubMed ID: 12214780
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  • 10. [Psychological aspects of Prader-Willi syndrome. Results of a parent survey].
    Sarimski K.
    Z Kinder Jugendpsychiatr; 1995 Dec; 23(4):267-74. PubMed ID: 8571685
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  • 13. Maladaptive behavior in children with Prader-Willi syndrome, Down syndrome, and nonspecific mental retardation.
    Dykens EM, Kasari C.
    Am J Ment Retard; 1997 Nov; 102(3):228-37. PubMed ID: 9394132
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  • 14. Maternal parenting stress in families with a child with Angelman syndrome or Prader-Willi syndrome.
    Wulffaert J, Scholte EM, Van Berckelaer-Onnes IA.
    J Intellect Dev Disabil; 2010 Sep; 35(3):165-74. PubMed ID: 20809878
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  • 17. Behavioural phenotypes and special educational needs: is aetiology important in the classroom?
    Reilly C.
    J Intellect Disabil Res; 2012 Oct; 56(10):929-46. PubMed ID: 22471356
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  • 18. 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
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  • 19. Clinical and behavioral characteristics in FG syndrome.
    Graham JM, Superneau D, Rogers RC, Corning K, Schwartz CE, Dykens EM.
    Am J Med Genet; 1999 Aug 27; 85(5):470-5. PubMed ID: 10405444
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