307 related articles for article (PubMed ID: 17573966)
1. Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromes.
Makoff AJ; Flomen RH
Genome Biol; 2007; 8(6):R114. PubMed ID: 17573966
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.
Amos-Landgraf JM; Ji Y; Gottlieb W; Depinet T; Wandstrat AE; Cassidy SB; Driscoll DJ; Rogan PK; Schwartz S; Nicholls RD
Am J Hum Genet; 1999 Aug; 65(2):370-86. PubMed ID: 10417280
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
Kalsner L; Chamberlain SJ
Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
[TBL] [Abstract][Full Text] [Related]
6. De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature.
Kitsiou-Tzeli S; Tzetis M; Sofocleous C; Vrettou C; Xaidara A; Giannikou K; Pampanos A; Mavrou A; Kanavakis E
Am J Med Genet A; 2010 Aug; 152A(8):1925-32. PubMed ID: 20575009
[TBL] [Abstract][Full Text] [Related]
7. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
Mignon-Ravix C; Depetris D; Luciani JJ; Cuoco C; Krajewska-Walasek M; Missirian C; Collignon P; Delobel B; Croquette MF; Moncla A; Kroisel PM; Mattei MG
Eur J Hum Genet; 2007 Apr; 15(4):432-40. PubMed ID: 17264869
[TBL] [Abstract][Full Text] [Related]
8. Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb.
Christian SL; Bhatt NK; Martin SA; Sutcliffe JS; Kubota T; Huang B; Mutirangura A; Chinault AC; Beaudet AL; Ledbetter DH
Genome Res; 1998 Feb; 8(2):146-57. PubMed ID: 9477342
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene.
Mutirangura A; Jayakumar A; Sutcliffe JS; Nakao M; McKinney MJ; Buiting K; Horsthemke B; Beaudet AL; Chinault AC; Ledbetter DH
Genomics; 1993 Dec; 18(3):546-52. PubMed ID: 8307564
[TBL] [Abstract][Full Text] [Related]
11. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
Christian SL; Robinson WP; Huang B; Mutirangura A; Line MR; Nakao M; Surti U; Chakravarti A; Ledbetter DH
Am J Hum Genet; 1995 Jul; 57(1):40-8. PubMed ID: 7611294
[TBL] [Abstract][Full Text] [Related]
12. Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13.
Dittrich B; Knoblauch H; Buiting K; Horsthemke B
Genomics; 1993 Apr; 16(1):269-71. PubMed ID: 8486372
[TBL] [Abstract][Full Text] [Related]
13. Characterisation of interstitial duplications and triplications of chromosome 15q11-q13.
Roberts SE; Dennis NR; Browne CE; Willatt L; Woods G; Cross I; Jacobs PA; Thomas S
Hum Genet; 2002 Mar; 110(3):227-34. PubMed ID: 11935334
[TBL] [Abstract][Full Text] [Related]
14. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
Leana-Cox J; Jenkins L; Palmer CG; Plattner R; Sheppard L; Flejter WL; Zackowski J; Tsien F; Schwartz S
Am J Hum Genet; 1994 May; 54(5):748-56. PubMed ID: 8178816
[TBL] [Abstract][Full Text] [Related]
15. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
Spinner NB; Zackai E; Cheng SD; Knoll JH
Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
[TBL] [Abstract][Full Text] [Related]
16. Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.
Aypar U; Brodersen PR; Lundquist PA; Dawson DB; Thorland EC; Hoppman N
Am J Med Genet A; 2014 Oct; 164A(10):2514-20. PubMed ID: 24975781
[TBL] [Abstract][Full Text] [Related]
17. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15.
Wang NJ; Parokonny AS; Thatcher KN; Driscoll J; Malone BM; Dorrani N; Sigman M; LaSalle JM; Schanen NC
BMC Genet; 2008 Jan; 9():2. PubMed ID: 18177502
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.
Wandstrat AE; Leana-Cox J; Jenkins L; Schwartz S
Am J Hum Genet; 1998 Apr; 62(4):925-36. PubMed ID: 9529335
[TBL] [Abstract][Full Text] [Related]
20. Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes.
Buiting K; Gross S; Ji Y; Senger G; Nicholls RD; Horsthemke B
Cytogenet Cell Genet; 1998; 81(3-4):247-53. PubMed ID: 9730612
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
