These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
507 related articles for article (PubMed ID: 9401540)
1. The genetic basis for Prader-Willi syndrome: the importance of imprinted genes. Brøndum-Nielsen K Acta Paediatr Suppl; 1997 Nov; 423():55-7. PubMed ID: 9401540 [TBL] [Abstract][Full Text] [Related]
2. [Prader-Willi syndrome and genomic imprinting]. Wang W; Wang DF; Cui YF; Ni JH; Dong ZY; Fu MF; Fu HM; Lu GQ; Chen FS Zhonghua Er Ke Za Zhi; 2003 Jun; 41(6):453-6. PubMed ID: 14749005 [TBL] [Abstract][Full Text] [Related]
3. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes. Glenn CC; Driscoll DJ; Yang TP; Nicholls RD Mol Hum Reprod; 1997 Apr; 3(4):321-32. PubMed ID: 9237260 [TBL] [Abstract][Full Text] [Related]
4. Imprinted genes in the Prader-Willi deletion. Francke U Novartis Found Symp; 1998; 214():264-75; discussion 275-9. PubMed ID: 9601023 [TBL] [Abstract][Full Text] [Related]
5. Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy? Smith A Acta Genet Med Gemellol (Roma); 1996; 45(1-2):179-89. PubMed ID: 8872029 [TBL] [Abstract][Full Text] [Related]
6. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint. Schulze A; Hansen C; Skakkebaek NE; Brøndum-Nielsen K; Ledbeter DH; Tommerup N Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505 [TBL] [Abstract][Full Text] [Related]
7. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome. Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639 [TBL] [Abstract][Full Text] [Related]
8. Genetic abnormalities in Prader-Willi syndrome and lessons from mouse models. Nicholls RD; Ohta T; Gray TA Acta Paediatr Suppl; 1999 Dec; 88(433):99-104. PubMed ID: 10626556 [TBL] [Abstract][Full Text] [Related]
9. 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 [TBL] [Abstract][Full Text] [Related]
11. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method. Zeschnigk M; Schmitz B; Dittrich B; Buiting K; Horsthemke B; Doerfler W Hum Mol Genet; 1997 Mar; 6(3):387-95. PubMed ID: 9147641 [TBL] [Abstract][Full Text] [Related]
12. Prader-Willi syndrome: reflections on seminal studies and future therapies. Chung MS; Langouët M; Chamberlain SJ; Carmichael GG Open Biol; 2020 Sep; 10(9):200195. PubMed ID: 32961075 [TBL] [Abstract][Full Text] [Related]
13. Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations. Saitoh S; Buiting K; Rogan PK; Buxton JL; Driscoll DJ; Arnemann J; König R; Malcolm S; Horsthemke B; Nicholls RD Proc Natl Acad Sci U S A; 1996 Jul; 93(15):7811-5. PubMed ID: 8755558 [TBL] [Abstract][Full Text] [Related]
14. Prader-Willi syndrome and Angelman syndrome. Buiting K Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):365-76. PubMed ID: 20803659 [TBL] [Abstract][Full Text] [Related]
15. Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome. Zilina O; Kahre T; Talvik I; Oiglane-Shlik E; Tillmann V; Ounap K Eur J Med Genet; 2014; 57(6):279-83. PubMed ID: 24704109 [TBL] [Abstract][Full Text] [Related]
16. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control. Lee S; Wevrick R Am J Hum Genet; 2000 Mar; 66(3):848-58. PubMed ID: 10712201 [TBL] [Abstract][Full Text] [Related]
17. Prader-Willi and Angelman syndromes. Disorders of genomic imprinting. Cassidy SB; Schwartz S Medicine (Baltimore); 1998 Mar; 77(2):140-51. PubMed ID: 9556704 [TBL] [Abstract][Full Text] [Related]
18. Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD. Muthusamy K; Macke EL; Klee EW; Tebben PJ; Hand JL; Hasadsri L; Marcou CA; Schimmenti LA Am J Med Genet A; 2020 Oct; 182(10):2442-2449. PubMed ID: 32815268 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2). Park JP; Moeschler JB; Hani VH; Hawk AB; Belloni DR; Noll WW; Mohandas TK Am J Med Genet; 1998 Jun; 78(2):134-9. PubMed ID: 9674903 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]