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Journal Abstract Search

307 related items for PubMed ID: 9972835

  • 1. Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy.
    Dykens EM, Cassidy SB, King BH.
    Am J Ment Retard; 1999 Jan; 104(1):67-77. PubMed ID: 9972835
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  • 3. 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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  • 5. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.
    Bittel DC, Kibiryeva N, Butler MG.
    Pediatrics; 2006 Oct; 118(4):e1276-83. PubMed ID: 16982806
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  • 7. Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: an ERP study.
    Stauder JE, Boer H, Gerits RH, Tummers A, Whittington J, Curfs LM.
    Clin Neurophysiol; 2005 Jun; 116(6):1464-70. PubMed ID: 15978509
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  • 9. The Prader-Willi syndrome and the Angelman syndrome.
    Vogels A, Fryns JP.
    Genet Couns; 2002 Jun; 13(4):385-96. PubMed ID: 12558108
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  • 10. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
    Camprubí C, Coll MD, Villatoro S, Gabau E, Kamli A, Martínez MJ, Poyatos D, Guitart M.
    Eur J Med Genet; 2007 Jun; 50(1):11-20. PubMed ID: 17095305
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  • 11. Sporadic occurrence of nondeletion Prader-Willi syndrome in two cases: a female with maternal uniparental disomy and a male with complex chromosomal rearrangement.
    Murthy SK, al-Nassar KE, Verghese L.
    Nutrition; 1995 Jun; 11(5 Suppl):650-2. PubMed ID: 8748243
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  • 12. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].
    Santa María L, Curotto B, Cortés F, Rojas C, Alliende MA.
    Rev Med Chil; 2001 Apr; 129(4):367-74. PubMed ID: 11413988
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  • 14. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
    Calounova G, Novotna D, Simandlova M, Havlovicova M, Zumrová A, Kocarek E, Sedlacek Z.
    Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828
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  • 16. Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15.
    Gunay-Aygun M, Heeger S, Schwartz S, Cassidy SB.
    Am J Med Genet; 1997 Jul 11; 71(1):106-10. PubMed ID: 9215778
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  • 19. Family studies in Prader-Willi syndrome.
    Webb T, Hardy CA, Dahlitz M, Watkiss E, Clarke D.
    Genet Couns; 1994 Jul 11; 5(4):329-36. PubMed ID: 7888134
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