331 related articles for article (PubMed ID: 19041960)
21. 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]
22. 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]
23. Post-zygotic breakage of a dicentric chromosome results in mosaicism for a telocentric 9p marker chromosome in a boy with developmental delay.
Pedurupillay CR; Misceo D; Gamage TH; Dissanayake VH; Frengen E
Gene; 2014 Jan; 533(1):403-10. PubMed ID: 24095780
[TBL] [Abstract][Full Text] [Related]
24. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction.
Chen CP; Ko TM; Huang WC; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Pan CW; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Jun; 55(3):415-8. PubMed ID: 27343326
[TBL] [Abstract][Full Text] [Related]
25. Inverted duplications deletions: underdiagnosed rearrangements??
Zuffardi O; Bonaglia M; Ciccone R; Giorda R
Clin Genet; 2009 Jun; 75(6):505-13. PubMed ID: 19508415
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. 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]
28. Masked complex chromosome rearrangement in a child thought to have del(8qter) as the sole cytogenetic abnormality.
Surace C; Digilio MC; Lombardo A; Sirleto P; Tomaiuolo AC; Roberti MC; Capolino R; Angioni A
Cytogenet Genome Res; 2008; 121(3-4):215-21. PubMed ID: 18758162
[TBL] [Abstract][Full Text] [Related]
29. 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
Barber JC; Maloney VK; Huang S; Bunyan DJ; Cresswell L; Kinning E; Benson A; Cheetham T; Wyllie J; Lynch SA; Zwolinski S; Prescott L; Crow Y; Morgan R; Hobson E
Eur J Hum Genet; 2008 Jan; 16(1):18-27. PubMed ID: 17940555
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Molecular cytogenetic characterization of the first reported case of inv dup del 20p compatible with a U-type exchange model.
Leclercq S; Maincent K; Baverel F; Tessier DL; Letourneur F; Lebbar A; Dupont JM
Am J Med Genet A; 2009 Mar; 149A(3):437-45. PubMed ID: 19206177
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. 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]
35. 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]
36. 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]
37. 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]
38. Independent post-zygotic breaks of a dicentric chromosome result in mosaicism for an inverted duplication deletion 9p and terminal deletion 9p.
Schlade-Bartusiak K; Tucker T; Safavi H; Livingston J; van Allen MI; Eydoux P; Armstrong L
Eur J Med Genet; 2013 May; 56(5):229-35. PubMed ID: 23416622
[TBL] [Abstract][Full Text] [Related]
39. Analysis of invdupdel(8p) rearrangement: Clinical, cytogenetic and molecular characterization.
García-Santiago FA; Martínez-Glez V; Santos F; García-Miñaur S; Mansilla E; Meneses AG; Rosell J; Granero ÁP; Vallespín E; Fernández L; Sierra B; Oliver-Bonet M; Palomares M; de Torres ML; Mori MÁ; Nevado J; Heath KE; Delicado A; Lapunzina P
Am J Med Genet A; 2015 May; 167A(5):1018-25. PubMed ID: 25712135
[TBL] [Abstract][Full Text] [Related]
40. The embryo battle against adverse genomes: Are de novo terminal deletions the rescue of unfavorable zygotic imbalances?
Zuffardi O; Fichera M; Bonaglia MC
Eur J Med Genet; 2022 Aug; 65(8):104532. PubMed ID: 35724817
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]