168 related articles for article (PubMed ID: 19041960)
1. Unusual 8p inverted duplication deletion with telomere capture from 8q.
Buysse K; Antonacci F; Callewaert B; Loeys B; Fränkel U; Siu V; Mortier G; Speleman F; Menten B
Eur J Med Genet; 2009; 52(1):31-6. PubMed ID: 19041960
[TBL] [Abstract][Full Text] [Related]
2. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
Guo WJ; Callif-Daley F; Zapata MC; Miller ME
Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
[TBL] [Abstract][Full Text] [Related]
3. Stabilization of a terminal inversion duplication of 8p by telomere capture from 18q.
Kostiner DR; Nguyen H; Cox VA; Cotter PD
Cytogenet Genome Res; 2002; 98(1):9-12. PubMed ID: 12584435
[TBL] [Abstract][Full Text] [Related]
4. [Inverted duplication of the short arm of chromosome 8].
Rodríguez Martínez L; Jiménez Muñoz-Delgado N; Nieto C; Martínez Carrascal A; López Grondona F; Martínez Frías ML
An Esp Pediatr; 2001 Nov; 55(5):458-62. PubMed ID: 11696311
[TBL] [Abstract][Full Text] [Related]
5. Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.
Barber JC; James RS; Patch C; Temple IK
Am J Med Genet; 1994 Apr; 50(3):296-9. PubMed ID: 8042676
[TBL] [Abstract][Full Text] [Related]
6. Inv dup(22), del(22)(q11) and r(22) in the father of a child with DiGeorge syndrome.
Bergman A; Blennow E
Eur J Hum Genet; 2000 Oct; 8(10):801-4. PubMed ID: 11039583
[TBL] [Abstract][Full Text] [Related]
7. Molecular characterization of inv dup del(8p): analysis of five cases.
Shimokawa O; Kurosawa K; Ida T; Harada N; Kondoh T; Miyake N; Yoshiura K; Kishino T; Ohta T; Niikawa N; Matsumoto N
Am J Med Genet A; 2004 Jul; 128A(2):133-7. PubMed ID: 15214003
[TBL] [Abstract][Full Text] [Related]
8. Inverted duplication of 8p: ten new patients and review of the literature.
Feldman GL; Weiss L; Phelan MC; Schroer RJ; Van Dyke DL
Am J Med Genet; 1993 Sep; 47(4):482-6. PubMed ID: 8256810
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements.
Giglio S; Broman KW; Matsumoto N; Calvari V; Gimelli G; Neumann T; Ohashi H; Voullaire L; Larizza D; Giorda R; Weber JL; Ledbetter DH; Zuffardi O
Am J Hum Genet; 2001 Apr; 68(4):874-83. PubMed ID: 11231899
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular cytogenetic characterization of a derivative chromosome 8 with an inverted duplication of 8p21.3-->p23.3 and a rearranged duplication of 8q24.13-->qter.
Fan YS; Siu VM
Am J Med Genet; 2001 Aug; 102(3):266-71. PubMed ID: 11484205
[TBL] [Abstract][Full Text] [Related]
13. Inverted tandem ("mirror") duplications in human chromosomes: -nv dup 8p, 4q, 22q.
Taylor KM; Francke U; Brown MG; George DL; Kaufhold M
Am J Med Genet; 1977; 1(1):3-19. PubMed ID: 610424
[TBL] [Abstract][Full Text] [Related]
14. A familial inverted duplication 2q33-q34 identified and delineated by multiple cytogenetic techniques.
Eussen BH; van de Laar I; Douben H; van Kempen L; Hochstenbach R; De Man SA; Van Opstal D; de Klein A; Poddighe PJ
Eur J Med Genet; 2007; 50(2):112-9. PubMed ID: 17161033
[TBL] [Abstract][Full Text] [Related]
15. Distal 8p deletion (8)(p23.1): an easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardation.
Wu BL; Schneider GH; Sabatino DE; Bozovic LZ; Cao B; Korf BR
Am J Med Genet; 1996 Mar; 62(1):77-83. PubMed ID: 8779331
[TBL] [Abstract][Full Text] [Related]
16. Complex CGH alterations on chromosome arm 8p at candidate tumor suppressor gene loci in breast cancer cell lines.
Venter DJ; Ramus SJ; Hammet FM; de Silva M; Hutchins AM; Petrovic V; Price G; Armes JE
Cancer Genet Cytogenet; 2005 Jul; 160(2):134-40. PubMed ID: 15993269
[TBL] [Abstract][Full Text] [Related]
17. Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.
Velinov M; Gu H; Genovese M; Duncan C; Warburton P; Brooks SS; Jenkins EC
Ann Genet; 2004; 47(2):199-205. PubMed ID: 15183754
[TBL] [Abstract][Full Text] [Related]
18. Sperm-FISH analysis in a pericentric chromosome 1 inversion, 46,XY,inv(1)(p22q42), associated with infertility.
Chantot-Bastaraud S; Ravel C; Berthaut I; McElreavey K; Bouchard P; Mandelbaum J; Siffroi JP
Mol Hum Reprod; 2007 Jan; 13(1):55-9. PubMed ID: 17077110
[TBL] [Abstract][Full Text] [Related]
19. Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.
Wyandt HE; Lebo RV; Fenerci EY; Sadhu DN; Milunsky JM
Am J Med Genet; 2000 Aug; 93(4):305-12. PubMed ID: 10946358
[TBL] [Abstract][Full Text] [Related]
20. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
de Die-Smulders CE; Engelen JJ; Schrander-Stumpel CT; Govaerts LC; de Vries B; Vles JS; Wagemans A; Schijns-Fleuren S; Gillessen-Kaesbach G; Fryns JP
Am J Med Genet; 1995 Nov; 59(3):369-74. PubMed ID: 8599364
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
