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4. 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; 66(4):368-72. PubMed ID: 15355442 [No Abstract] [Full Text] [Related]
5. 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 [TBL] [Abstract][Full Text] [Related]
6. An immunological basis of hyperphagia driven by GABAergic dysfunction in Prader-Willi Syndrome. Rout U; Abdul-Rahman OA; Dhossche DM Med Hypotheses; 2012 Apr; 78(4):462-4. PubMed ID: 22289342 [TBL] [Abstract][Full Text] [Related]
7. Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy. Boer H; Holland A; Whittington J; Butler J; Webb T; Clarke D Lancet; 2002 Jan; 359(9301):135-6. PubMed ID: 11809260 [TBL] [Abstract][Full Text] [Related]
8. 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; 72(4):378-80. PubMed ID: 17850637 [No Abstract] [Full Text] [Related]
9. Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome. Salavoura K; Kolialexi A; Sofocleous C; Kalaitzidaki M; Pampanos A; Kitsiou S; Mavrou A Genet Couns; 2008; 19(2):219-24. PubMed ID: 18618997 [TBL] [Abstract][Full Text] [Related]
10. [To know more about the Prader-Willi syndrome. Diagnosis]. Midro AT; Olchowik B; Lebiedzińska A; Midro H Psychiatr Pol; 2009; 43(2):135-49. PubMed ID: 19697784 [TBL] [Abstract][Full Text] [Related]
11. A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15. Giardina E; Peconi C; Cascella R; Sinibaldi C; Nardone AM; Novelli G Electrophoresis; 2008 Dec; 29(23):4775-9. PubMed ID: 19053076 [TBL] [Abstract][Full Text] [Related]
12. Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes. Horsthemke B; Nazlican H; Hüsing J; Klein-Hitpass L; Claussen U; Michel S; Lich C; Gillessen-Kaesbach G; Buiting K Hum Mol Genet; 2003 Oct; 12(20):2723-32. PubMed ID: 12944418 [TBL] [Abstract][Full Text] [Related]
13. Neurobehavioral phenotype in Prader-Willi syndrome. Whittington J; Holland A Am J Med Genet C Semin Med Genet; 2010 Nov; 154C(4):438-47. PubMed ID: 20981773 [TBL] [Abstract][Full Text] [Related]
14. Advanced maternal age at childbirth and the development of uniparental disomy. A commentary on the proportion of uniparental disomy is increased in Prader-Willi syndrome due to an advanced maternal childbearing age in Korea. Matsubara K; Ogata T J Hum Genet; 2013 Mar; 58(3):118-9. PubMed ID: 23364392 [No Abstract] [Full Text] [Related]
16. A twin sibling with Prader-Willi syndrome caused by uniparental disomy conceived after in vitro fertilization. Atik T; Aykut A; Karaca E; Onay H; Ozkinay F; Cogulu O Genet Couns; 2014; 25(4):433-7. PubMed ID: 25804024 [TBL] [Abstract][Full Text] [Related]
17. [Genomic imprinting in Prader-Willi syndrome]. Szpecht-Potocka A Postepy Biochem; 2001; 47(1):87-97. PubMed ID: 11503444 [No Abstract] [Full Text] [Related]
18. 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 [TBL] [Abstract][Full Text] [Related]
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20. Genetics and mathematics: evidence from Prader-Willi syndrome. Semenza C; Pignatti R; Bertella L; Ceriani F; Mori I; Molinari E; Giardino D; Malvestiti F; Grugni G Neuropsychologia; 2008 Jan; 46(1):206-12. PubMed ID: 17845808 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]