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Results: 1 to 20 of 107

1.

Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.

Gold JA, Ruth C, Osann K, Flodman P, McManus B, Lee HS, Donkervoort S, Khare M, Roof E, Dykens E, Miller JL, Driscoll DJ, Butler MG, Heinemann J, Cassidy S, Kimonis VE.

Genet Med. 2014 Feb;16(2):164-9. doi: 10.1038/gim.2013.97. Epub 2013 Aug 8. Erratum in: Genet Med. 2013 Nov;15(11):912. Miller, Jennifer L [added].

PMID:
23928912
[PubMed - in process]
2.

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. Epub 2006 Sep 18.

PMID:
16982806
[PubMed - indexed for MEDLINE]
Free Article
3.

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. doi: 10.1002/ajmg.a.35549. Epub 2012 Aug 17.

PMID:
22903639
[PubMed - indexed for MEDLINE]
4.

The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.

Gunay-Aygun M, Schwartz S, Heeger S, O'Riordan MA, Cassidy SB.

Pediatrics. 2001 Nov;108(5):E92.

PMID:
11694676
[PubMed - indexed for MEDLINE]
5.

The genetic basis for Prader-Willi syndrome: the importance of imprinted genes.

Brøndum-Nielsen K.

Acta Paediatr Suppl. 1997 Nov;423:55-7.

PMID:
9401540
[PubMed - indexed for MEDLINE]
6.

Assisted reproductive technology surveillance -- United States, 2010.

Sunderam S, Kissin DM, Crawford S, Anderson JE, Folger SG, Jamieson DJ, Barfield WD; Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, CDC.

MMWR Surveill Summ. 2013 Dec 6;62(9):1-24.

PMID:
24304902
[PubMed - indexed for MEDLINE]
Free Article
7.

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

Mascari MJ, Gottlieb W, Rogan PK, Butler MG, Waller DA, Armour JA, Jeffreys AJ, Ladda RL, Nicholls RD.

N Engl J Med. 1992 Jun 11;326(24):1599-607.

PMID:
1584261
[PubMed - indexed for MEDLINE]
Free Article
8.

Prader-Willi Syndrome: Obesity due to Genomic Imprinting.

Butler MG.

Curr Genomics. 2011 May;12(3):204-15. doi: 10.2174/138920211795677877.

PMID:
22043168
[PubMed]
Free PMC Article
9.

Prader-Willi Syndrome With a Long-Contiguous Stretch of Homozygosity Not Covering the Critical Region.

Yingjun X, Yi Z, Jianzhu W, Yunxia S, Yongzhen C, Liangying Z, Xiangyi J, Qun F.

J Child Neurol. 2014 May 22. pii: 0883073814535492. [Epub ahead of print]

PMID:
24859787
[PubMed - as supplied by publisher]
10.

Prader-Willi syndrome.

Cassidy SB, Schwartz S, Miller JL, Driscoll DJ.

Genet Med. 2012 Jan;14(1):10-26. doi: 10.1038/gim.0b013e31822bead0. Epub 2011 Sep 26. Review.

PMID:
22237428
[PubMed - indexed for MEDLINE]
11.

Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.

Bittel DC, Butler MG.

Expert Rev Mol Med. 2005 Jul 25;7(14):1-20. Review.

PMID:
16038620
[PubMed - indexed for MEDLINE]
12.

Prader-Willi syndrome.

Cassidy SB, Schwartz S, Miller JL, Driscoll DJ.

Genet Med. 2011 Sep 26. [Epub ahead of print]

PMID:
21952424
[PubMed - as supplied by publisher]
13.

Assisted reproductive technology surveillance--United States, 2009.

Sunderam S, Kissin DM, Flowers L, Anderson JE, Folger SG, Jamieson DJ, Barfield WD; Centers for Disease Control and Prevention (CDC).

MMWR Surveill Summ. 2012 Nov 2;61(7):1-23.

PMID:
23114281
[PubMed - indexed for MEDLINE]
Free Article
14.

Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.

Cassidy SB, Schwartz S.

Medicine (Baltimore). 1998 Mar;77(2):140-51. Review.

PMID:
9556704
[PubMed - indexed for MEDLINE]
15.

Mosaic maternal uniparental disomy of chromosome 15 in Prader-Willi syndrome: utility of genome-wide SNP array.

Izumi K, Santani AB, Deardorff MA, Feret HA, Tischler T, Thiel BD, Mulchandani S, Stolle CA, Spinner NB, Zackai EH, Conlin LK.

Am J Med Genet A. 2013 Jan;161A(1):166-71. doi: 10.1002/ajmg.a.35625. Epub 2012 Dec 7.

PMID:
23225330
[PubMed - indexed for MEDLINE]
16.

Psychiatric disorders in Prader-Willi syndrome: epidemiology and management.

Dykens E, Shah B.

CNS Drugs. 2003;17(3):167-78. Review.

PMID:
12617696
[PubMed - indexed for MEDLINE]
17.

Clinical features and molecular genetic analysis of a boy with Prader-Willi syndrome caused by an imprinting defect.

Schulze A, Hansen C, Baekgaard P, Blichfeldt S, Petersen MB, Tommerup N, Brøndum-Nielsen K.

Acta Paediatr. 1997 Aug;86(8):906-10.

PMID:
9307178
[PubMed - indexed for MEDLINE]
18.

Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes.

Boyle J, Hawkins M, Barton DE, Meaney K, Guitart M, O'Grady A, Tobi S, Ramsden SC, Elles R, Gray E, Metcalfe P, Hawkins JR.

Eur J Hum Genet. 2011 Aug;19(8):857-64. doi: 10.1038/ejhg.2011.59. Epub 2011 May 18.

PMID:
21587322
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Imprinted genes in the Prader-Willi deletion.

Francke U.

Novartis Found Symp. 1998;214:264-75; discussion 275-9. Review.

PMID:
9601023
[PubMed - indexed for MEDLINE]
20.

Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.

Conroy JM, Grebe TA, Becker LA, Tsuchiya K, Nicholls RD, Buiting K, Horsthemke B, Cassidy SB, Schwartz S.

Am J Hum Genet. 1997 Aug;61(2):388-94.

PMID:
9311744
[PubMed - indexed for MEDLINE]
Free PMC Article

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