245 related articles for article (PubMed ID: 11156619)
1. Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26.
Pujana MA; Nadal M; Gratacòs M; Peral B; Csiszar K; González-Sarmiento R; Sumoy L; Estivill X
Genome Res; 2001 Jan; 11(1):98-111. PubMed ID: 11156619
[TBL] [Abstract][Full Text] [Related]
2. Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons.
Pujana MA; Nadal M; Guitart M; Armengol L; Gratacòs M; Estivill X
Eur J Hum Genet; 2002 Jan; 10(1):26-35. PubMed ID: 11896453
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.
Jiang YH; Wauki K; Liu Q; Bressler J; Pan Y; Kashork CD; Shaffer LG; Beaudet AL
BMC Genomics; 2008 Jan; 9():50. PubMed ID: 18226259
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.
Chai JH; Locke DP; Greally JM; Knoll JH; Ohta T; Dunai J; Yavor A; Eichler EE; Nicholls RD
Am J Hum Genet; 2003 Oct; 73(4):898-925. PubMed ID: 14508708
[TBL] [Abstract][Full Text] [Related]
7. 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]
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. The human gene for the poly(A)-specific ribonuclease (PARN) maps to 16p13 and has a truncated copy in the Prader-Willi/Angelman syndrome region on 15q11-->q13.
Buiting K; Körner C; Ulrich B; Wahle E; Horsthemke B
Cytogenet Cell Genet; 1999; 87(1-2):125-31. PubMed ID: 10640832
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human.
Ji Y; Rebert NA; Joslin JM; Higgins MJ; Schultz RA; Nicholls RD
Genome Res; 2000 Mar; 10(3):319-29. PubMed ID: 10720573
[TBL] [Abstract][Full Text] [Related]
12. Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.
Maddox LO; Menold MM; Bass MP; Rogala AR; Pericak-Vance MA; Vance JM; Gilbert JR
Genomics; 1999 Dec; 62(3):325-31. PubMed ID: 10644429
[TBL] [Abstract][Full Text] [Related]
13. Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures.
Sutcliffe JS; Han MK; Amin T; Kesterson RA; Nurmi EL
BMC Genomics; 2003 Apr; 4(1):15. PubMed ID: 12720574
[TBL] [Abstract][Full Text] [Related]
14. Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangements.
Sahoo T; Shaw CA; Young AS; Whitehouse NL; Schroer RJ; Stevenson RE; Beaudet AL
Am J Med Genet A; 2005 Dec; 139A(2):106-13. PubMed ID: 16284940
[TBL] [Abstract][Full Text] [Related]
15. Proximal 15q familial euchromatic variant and PWS/AS critical region duplication in the same patient: a cytogenetic pitfall.
Carelle-Calmels N; Girard-Lemaire F; Guérin E; Bieth E; Rudolf G; Biancalana V; Pecheur H; Demil H; Schneider T; de Saint-Martin A; Caron O; Legrain M; Gaston V; Flori E
Eur J Med Genet; 2008; 51(6):547-57. PubMed ID: 18692163
[TBL] [Abstract][Full Text] [Related]
16. A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications.
Ritchie RJ; Mattei MG; Lalande M
Hum Mol Genet; 1998 Aug; 7(8):1253-60. PubMed ID: 9668167
[TBL] [Abstract][Full Text] [Related]
17. High-resolution molecular characterization of 15q11-q13 rearrangements by array comparative genomic hybridization (array CGH) with detection of gene dosage.
Wang NJ; Liu D; Parokonny AS; Schanen NC
Am J Hum Genet; 2004 Aug; 75(2):267-81. PubMed ID: 15197683
[TBL] [Abstract][Full Text] [Related]
18. A novel ETV6-NTRK3 gene fusion in congenital fibrosarcoma.
Knezevich SR; McFadden DE; Tao W; Lim JF; Sorensen PH
Nat Genet; 1998 Feb; 18(2):184-7. PubMed ID: 9462753
[TBL] [Abstract][Full Text] [Related]
19. Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25.
Ventura M; Mudge JM; Palumbo V; Burn S; Blennow E; Pierluigi M; Giorda R; Zuffardi O; Archidiacono N; Jackson MS; Rocchi M
Genome Res; 2003 Sep; 13(9):2059-68. PubMed ID: 12915487
[TBL] [Abstract][Full Text] [Related]
20. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
Nicholls RD; Knepper JL
Annu Rev Genomics Hum Genet; 2001; 2():153-75. PubMed ID: 11701647
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]