212 related articles for article (PubMed ID: 16628498)
1. Characterization of a complex rearrangement with interstitial deletions and inversion on human chromosome 1.
Gajecka M; Glotzbach CD; Shaffer LG
Chromosome Res; 2006; 14(3):277-82. PubMed ID: 16628498
[TBL] [Abstract][Full Text] [Related]
2. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
Ballif BC; Wakui K; Gajecka M; Shaffer LG
Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
[TBL] [Abstract][Full Text] [Related]
3. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.
Ballif BC; Yu W; Shaw CA; Kashork CD; Shaffer LG
Hum Mol Genet; 2003 Sep; 12(17):2153-65. PubMed ID: 12915474
[TBL] [Abstract][Full Text] [Related]
4. Monosomy 1p36 breakpoints indicate repetitive DNA sequence elements may be involved in generating and/or stabilizing some terminal deletions.
Ballif BC; Gajecka M; Shaffer LG
Chromosome Res; 2004; 12(2):133-41. PubMed ID: 15053483
[TBL] [Abstract][Full Text] [Related]
5. Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome.
Heilstedt HA; Ballif BC; Howard LA; Lewis RA; Stal S; Kashork CD; Bacino CA; Shapira SK; Shaffer LG
Am J Hum Genet; 2003 May; 72(5):1200-12. PubMed ID: 12687501
[TBL] [Abstract][Full Text] [Related]
6. FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.
Ballif BC; Kashork CD; Shaffer LG
Eur J Hum Genet; 2000 Oct; 8(10):764-70. PubMed ID: 11039576
[TBL] [Abstract][Full Text] [Related]
7. Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
Lennon PA; Cooper ML; Curtis MA; Lim C; Ou Z; Patel A; Cheung SW; Bacino CA
Am J Med Genet A; 2006 Jun; 140(11):1156-63. PubMed ID: 16688748
[TBL] [Abstract][Full Text] [Related]
8. Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.
Yatsenko SA; Brundage EK; Roney EK; Cheung SW; Chinault AC; Lupski JR
Hum Mol Genet; 2009 Jun; 18(11):1924-36. PubMed ID: 19293338
[TBL] [Abstract][Full Text] [Related]
9. Molecular-cytogenetic detection of a deletion of 1p36.3.
Giraudeau F; Aubert D; Young I; Horsley S; Knight S; Kearney L; Vergnaud G; Flint J
J Med Genet; 1997 Apr; 34(4):314-7. PubMed ID: 9138156
[TBL] [Abstract][Full Text] [Related]
10. Recurrent interstitial 1p36 deletions: Evidence for germline mosaicism and complex rearrangement breakpoints.
Gajecka M; Saitta SC; Gentles AJ; Campbell L; Ciprero K; Geiger E; Catherwood A; Rosenfeld JA; Shaikh T; Shaffer LG
Am J Med Genet A; 2010 Dec; 152A(12):3074-83. PubMed ID: 21108392
[TBL] [Abstract][Full Text] [Related]
11. Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.
Gajecka M; Glotzbach CD; Jarmuz M; Ballif BC; Shaffer LG
Eur J Hum Genet; 2006 Dec; 14(12):1255-62. PubMed ID: 16941016
[TBL] [Abstract][Full Text] [Related]
12. Identification of sequence motifs at the breakpoint junctions in three t(1;9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.
Gajecka M; Pavlicek A; Glotzbach CD; Ballif BC; Jarmuz M; Jurka J; Shaffer LG
Hum Genet; 2006 Nov; 120(4):519-26. PubMed ID: 16847692
[TBL] [Abstract][Full Text] [Related]
13. Further delineation of nonhomologous-based recombination and evidence for subtelomeric segmental duplications in 1p36 rearrangements.
D'Angelo CS; Gajecka M; Kim CA; Gentles AJ; Glotzbach CD; Shaffer LG; Koiffmann CP
Hum Genet; 2009 Jun; 125(5-6):551-63. PubMed ID: 19271239
[TBL] [Abstract][Full Text] [Related]
14. Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4.
Cotter PD; Kaffe S; Li L; Gershin IF; Hirschhorn K
Am J Med Genet; 2001 Jul; 102(1):76-80. PubMed ID: 11471177
[TBL] [Abstract][Full Text] [Related]
15. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
[TBL] [Abstract][Full Text] [Related]
16. An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA.
Katz SG; Schneider SS; Bartuski A; Trask BJ; Massa H; Overhauser J; Lalande M; Lansdorp PM; Silverman GA
Hum Mol Genet; 1999 Jan; 8(1):87-92. PubMed ID: 9887335
[TBL] [Abstract][Full Text] [Related]
17. Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions.
Yu W; Ballif BC; Kashork CD; Heilstedt HA; Howard LA; Cai WW; White LD; Liu W; Beaudet AL; Bejjani BA; Shaw CA; Shaffer LG
Hum Mol Genet; 2003 Sep; 12(17):2145-52. PubMed ID: 12915473
[TBL] [Abstract][Full Text] [Related]
18. FISH analysis of hematological neoplasias with 1p36 rearrangements allows the definition of a cluster of 2.5 Mb included in the minimal region deleted in 1p36 deletion syndrome.
Lahortiga I; Vázquez I; Belloni E; Román JP; Gasparini P; Novo FJ; Zudaire I; Pelicci PG; Hernández JM; Calasanz MJ; Odero MD
Hum Genet; 2005 May; 116(6):476-85. PubMed ID: 15744521
[TBL] [Abstract][Full Text] [Related]
19. Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.
Shaikh TH; O'Connor RJ; Pierpont ME; McGrath J; Hacker AM; Nimmakayalu M; Geiger E; Emanuel BS; Saitta SC
Genome Res; 2007 Apr; 17(4):482-91. PubMed ID: 17351135
[TBL] [Abstract][Full Text] [Related]
20. Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.
Chuzhanova N; Abeysinghe SS; Krawczak M; Cooper DN
Hum Mutat; 2003 Sep; 22(3):245-51. PubMed ID: 12938089
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]