150 related articles for article (PubMed ID: 18698613)
1. Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array.
Newkirk HL; Bittel DC; Butler MG
Am J Med Genet A; 2008 Sep; 146A(18):2346-54. PubMed ID: 18698613
[TBL] [Abstract][Full Text] [Related]
2. Determination of genomic copy number with quantitative microsphere hybridization.
Newkirk HL; Rogan PK; Miralles M; Knoll JH
Hum Mutat; 2006 Apr; 27(4):376-86. PubMed ID: 16541397
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.
Procter M; Chou LS; Tang W; Jama M; Mao R
Clin Chem; 2006 Jul; 52(7):1276-83. PubMed ID: 16690734
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.
Hassan M; Butler MG
Eur J Med Genet; 2016 Nov; 59(11):584-589. PubMed ID: 27659713
[TBL] [Abstract][Full Text] [Related]
7. Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome.
Tantravahi U; Nicholls RD; Stroh H; Ringer S; Neve RL; Kaplan L; Wharton R; Wurster-Hill D; Graham JM; CantĂș ES
Am J Med Genet; 1989 May; 33(1):78-87. PubMed ID: 2750788
[TBL] [Abstract][Full Text] [Related]
8. Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome.
Butler MG; Fischer W; Kibiryeva N; Bittel DC
Am J Med Genet A; 2008 Apr; 146A(7):854-60. PubMed ID: 18266248
[TBL] [Abstract][Full Text] [Related]
9. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
Christian SL; Fantes JA; Mewborn SK; Huang B; Ledbetter DH
Hum Mol Genet; 1999 Jun; 8(6):1025-37. PubMed ID: 10332034
[TBL] [Abstract][Full Text] [Related]
10. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
Nicholls RD; Knoll JH; Glatt K; Hersh JH; Brewster TD; Graham JM; Wurster-Hill D; Wharton R; Latt SA
Am J Med Genet; 1989 May; 33(1):66-77. PubMed ID: 2568752
[TBL] [Abstract][Full Text] [Related]
11. Influence of the Prader-Willi syndrome imprinting center on the DNA methylation landscape in the mouse brain.
Brant JO; Riva A; Resnick JL; Yang TP
Epigenetics; 2014 Nov; 9(11):1540-56. PubMed ID: 25482058
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
Hartin SN; Hossain WA; Weisensel N; Butler MG
Am J Med Genet A; 2018 Apr; 176(4):886-895. PubMed ID: 29437285
[TBL] [Abstract][Full Text] [Related]
14. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.
Gregory CA; Kirkilionis AJ; Greenberg CR; Chudley AE; Hamerton JL
Am J Med Genet; 1990 Apr; 35(4):536-45. PubMed ID: 1970703
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
Kuwano A; Mutirangura A; Dittrich B; Buiting K; Horsthemke B; Saitoh S; Niikawa N; Ledbetter SA; Greenberg F; Chinault AC
Hum Mol Genet; 1992 Sep; 1(6):417-25. PubMed ID: 1363801
[TBL] [Abstract][Full Text] [Related]
17. Detection of chromosome 15 deletion in Prader-Willi syndrome using fluorescence in situ hybridization.
Suzuki Y; Sasagawa I; Yazawa H; Tateno T; Nakada T
Arch Androl; 2000; 45(1):13-7. PubMed ID: 10959497
[TBL] [Abstract][Full Text] [Related]
18. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
Stefan M; Portis T; Longnecker R; Nicholls RD
Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315
[TBL] [Abstract][Full Text] [Related]
19. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
Clayton-Smith J; Driscoll DJ; Waters MF; Webb T; Andrews T; Malcolm S; Pembrey ME; Nicholls RD
Am J Med Genet; 1993 Oct; 47(5):683-6. PubMed ID: 8266996
[TBL] [Abstract][Full Text] [Related]
20. A molecular deletion study with southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11-12 and on an atypical PWS patient with apparently normal karyotype.
Kamei T; Hamabe JI; Matsumoto T; Abe K; Harada N; Ishikiriyama S; Hasegawa T; Miyazaki K; Mizuno S; Narahara K
Jinrui Idengaku Zasshi; 1988 Dec; 33(4):477-86. PubMed ID: 2907997
[No Abstract] [Full Text] [Related]
[Next] [New Search]