239 related articles for article (PubMed ID: 31225937)
1. Birth seasonality studies in a large Prader-Willi syndrome cohort.
Butler MG; Kimonis V; Dykens E; Gold JA; Tamura R; Miller JL; Driscoll DJ
Am J Med Genet A; 2019 Aug; 179(8):1531-1534. PubMed ID: 31225937
[TBL] [Abstract][Full Text] [Related]
2. Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study.
Butler MG; Hartin SN; Hossain WA; Manzardo AM; Kimonis V; Dykens E; Gold JA; Kim SJ; Weisensel N; Tamura R; Miller JL; Driscoll DJ
J Med Genet; 2019 Mar; 56(3):149-153. PubMed ID: 29730598
[TBL] [Abstract][Full Text] [Related]
3. Changing rates of genetic subtypes of Prader-Willi syndrome in the UK.
Whittington JE; Butler JV; Holland AJ
Eur J Hum Genet; 2007 Jan; 15(1):127-30. PubMed ID: 16957680
[TBL] [Abstract][Full Text] [Related]
4. Combined cytogenetic and molecular analyses for the diagnosis of Prader-Willi/Angelman syndromes.
Borelina D; Engel N; Esperante S; Ferreiro V; Ferrer M; Torrado M; Goldschmidt E; Francipane L; Szijan I
J Biochem Mol Biol; 2004 Sep; 37(5):522-6. PubMed ID: 15479613
[TBL] [Abstract][Full Text] [Related]
5. Is gestation in Prader-Willi syndrome affected by the genetic subtype?
Butler MG; Sturich J; Myers SE; Gold JA; Kimonis V; Driscoll DJ
J Assist Reprod Genet; 2009 Aug; 26(8):461-6. PubMed ID: 19760168
[TBL] [Abstract][Full Text] [Related]
6. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.
Robinson WP; Bottani A; Xie YG; Balakrishman J; Binkert F; Mächler M; Prader A; Schinzel A
Am J Hum Genet; 1991 Dec; 49(6):1219-34. PubMed ID: 1684085
[TBL] [Abstract][Full Text] [Related]
7. Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes.
Kim SJ; Miller JL; Kuipers PJ; German JR; Beaudet AL; Sahoo T; Driscoll DJ
Eur J Hum Genet; 2012 Mar; 20(3):283-90. PubMed ID: 22045295
[TBL] [Abstract][Full Text] [Related]
8. A girl with incomplete Prader-Willi syndrome and negative MS-PCR, found to have mosaic maternal UPD-15 at SNP array.
Morandi A; Bonnefond A; Lobbens S; Carotenuto M; Del Giudice EM; Froguel P; Maffeis C
Am J Med Genet A; 2015 Nov; 167A(11):2720-6. PubMed ID: 26109092
[TBL] [Abstract][Full Text] [Related]
9. Parental exposure to hydrocarbons in Prader-Willi syndrome.
Akefeldt A; Anvret M; Grandell U; Nordlinder R; Gillberg C
Dev Med Child Neurol; 1995 Dec; 37(12):1101-9. PubMed ID: 8566468
[TBL] [Abstract][Full Text] [Related]
10. Analysis of imprinted genes in subjects with Prader-Willi syndrome and chromosome 15 abnormalities.
Muralidhar B; Marney A; Butler MG
Genet Med; 1999; 1(4):141-5. PubMed ID: 11258349
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Deletions and duplications of the 15q11-q13 region in spermatozoa from Prader-Willi syndrome fathers.
Molina O; Blanco J; Vidal F
Mol Hum Reprod; 2010 May; 16(5):320-8. PubMed ID: 20083560
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Newborn screening for Prader-Willi syndrome is feasible: Early diagnosis for better outcomes.
Mahmoud R; Singh P; Weiss L; Lakatos A; Oakes M; Hossain W; Butler MG; Kimonis V
Am J Med Genet A; 2019 Jan; 179(1):29-36. PubMed ID: 30556641
[TBL] [Abstract][Full Text] [Related]
15. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
Gilhuis HJ; van Ravenswaaij CM; Hamel BJ; Gabreëls FJ
Eur J Paediatr Neurol; 2000; 4(1):39-43. PubMed ID: 10701104
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.
Driscoll DJ; Waters MF; Williams CA; Zori RT; Glenn CC; Avidano KM; Nicholls RD
Genomics; 1992 Aug; 13(4):917-24. PubMed ID: 1505981
[TBL] [Abstract][Full Text] [Related]
18. Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype.
Milner KM; Craig EE; Thompson RJ; Veltman MW; Thomas NS; Roberts S; Bellamy M; Curran SR; Sporikou CM; Bolton PF
J Child Psychol Psychiatry; 2005 Oct; 46(10):1089-96. PubMed ID: 16178933
[TBL] [Abstract][Full Text] [Related]
19. Clinical correlates of chromosome 15 deletions and maternal disomy in Prader-Willi syndrome.
Lai LW; Erickson RP; Cassidy SB
Am J Dis Child; 1993 Nov; 147(11):1217-23. PubMed ID: 7901987
[TBL] [Abstract][Full Text] [Related]
20. Chromosomal Microarray Study in Prader-Willi Syndrome.
Butler MG; Hossain WA; Cowen N; Bhatnagar A
Int J Mol Sci; 2023 Jan; 24(2):. PubMed ID: 36674736
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]