304 related articles for article (PubMed ID: 20083560)
1. 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]
2. Parental and chromosomal origins of microdeletion and duplication syndromes involving 7q11.23, 15q11-q13 and 22q11.
Thomas NS; Durkie M; Potts G; Sandford R; Van Zyl B; Youings S; Dennis NR; Jacobs PA
Eur J Hum Genet; 2006 Jul; 14(7):831-7. PubMed ID: 16617304
[TBL] [Abstract][Full Text] [Related]
3. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
[TBL] [Abstract][Full Text] [Related]
4. Sperm rates of 7q11.23, 15q11q13 and 22q11.2 deletions and duplications: a FISH approach.
Molina O; Anton E; Vidal F; Blanco J
Hum Genet; 2011 Jan; 129(1):35-44. PubMed ID: 20931230
[TBL] [Abstract][Full Text] [Related]
5. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.
Flori E; Biancalana V; Girard-Lemaire F; Favre R; Flori J; Doray B; Mandel JL
Eur J Hum Genet; 2004 Mar; 12(3):181-6. PubMed ID: 14694357
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.
Delach JA; Rosengren SS; Kaplan L; Greenstein RM; Cassidy SB; Benn PA
Am J Med Genet; 1994 Aug; 52(1):85-91. PubMed ID: 7977469
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
Engelen JJ; Loots WJ; Albrechts JC; Schrander-Stumpel CT; Dirckx R; Smeets HJ; Hamers AJ; Geraedts JP
Genet Couns; 1999; 10(2):123-32. PubMed ID: 10422004
[TBL] [Abstract][Full Text] [Related]
11. FISH analysis in Prader-Willi and Angelman syndrome patients.
Bettio D; Rizzi N; Giardino D; Grugni G; Briscioli V; Selicorni A; Carnevale F; Larizza L
Am J Med Genet; 1995 Mar; 56(2):224-8. PubMed ID: 7625450
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
Nicholls RD
Am J Med Genet; 1993 Apr; 46(1):16-25. PubMed ID: 8388169
[TBL] [Abstract][Full Text] [Related]
14. The mechanisms involved in formation of deletions and duplications of 15q11-q13.
Robinson WP; Dutly F; Nicholls RD; Bernasconi F; Peñaherrera M; Michaelis RC; Abeliovich D; Schinzel AA
J Med Genet; 1998 Feb; 35(2):130-6. PubMed ID: 9580159
[TBL] [Abstract][Full Text] [Related]
15. [Methylation-specific multiplex ligation-dependent probe amplification in diagnosis of Prader-Willi syndrome and Angelman syndrome].
Li MR; Wang XZ; Liu XY; Yang YL; Bao XH; Zhang YH; Xiong H; Zhong N; Qin J; Wu XR; Pan H
Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3257-61. PubMed ID: 19159549
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. True telomeric translocation in a baby with the Prader-Willi phenotype.
Reeve A; Norman A; Sinclair P; Whittington-Smith R; Hamey Y; Donnai D; Read A
Am J Med Genet; 1993 Aug; 47(1):1-6. PubMed ID: 8368237
[TBL] [Abstract][Full Text] [Related]
18. High rates of de novo 15q11q13 inversions in human spermatozoa.
Molina O; Anton E; Vidal F; Blanco J
Mol Cytogenet; 2012 Feb; 5(1):11. PubMed ID: 22309495
[TBL] [Abstract][Full Text] [Related]
19. Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men.
Kinoshita T; Mikami M; Ayabe T; Matsubara K; Ono H; Ohki K; Fukami M; Katoh-Fukui Y
Cytogenet Genome Res; 2019; 159(2):66-73. PubMed ID: 31639787
[TBL] [Abstract][Full Text] [Related]
20. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
Klein OD; Cotter PD; Albertson DG; Pinkel D; Tidyman WE; Moore MW; Rauen KA
Clin Genet; 2004 Jun; 65(6):477-82. PubMed ID: 15151506
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]