120 related articles for article (PubMed ID: 18160796)
1. A neocentromere derived from a supernumerary marker deleted from the long arm of chromosome 6.
Qin N; Bartley J; Wang JC; Warburton PE
Cytogenet Genome Res; 2007; 119(1-2):154-7. PubMed ID: 18160796
[TBL] [Abstract][Full Text] [Related]
2. Small supernumerary marker chromosome derived from proximal p-arm of chromosome 2: identification by fluorescent in situ hybridization.
Lasan Trcić R; Hitrec V; Letica L; Cuk M; Begović D
Croat Med J; 2003 Aug; 44(4):477-9. PubMed ID: 12950153
[TBL] [Abstract][Full Text] [Related]
3. Complementary duplication and deletion of 17 (pcen----p11.2): a family with a supernumerary chromosome comprised of an interstitially deleted segment.
Friedman JM; Harrod MJ; Howard-Peebles PN
Am J Med Genet; 1992 Sep; 44(1):37-40. PubMed ID: 1519647
[TBL] [Abstract][Full Text] [Related]
4. Interstitial deletion of proximal 8q including part of the centromere from unbalanced segregation of a paternal deletion/marker karyotype with neocentromere formation at 8p22.
Burnside RD; Ibrahim J; Flora C; Schwartz S; Tepperberg JH; Papenhausen PR; Warburton PE
Cytogenet Genome Res; 2011; 132(4):227-32. PubMed ID: 21212645
[TBL] [Abstract][Full Text] [Related]
5. Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report.
Brisset S; Izard V; Misrahi M; Aboura A; Madoux S; Ferlicot S; Schoevaert D; Soufir JC; Frydman R; Tachdjian G
Hum Reprod; 2005 Aug; 20(8):2168-72. PubMed ID: 15845593
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 -->13q22 chromosome and balancing reciprocal deletion.
Knegt AC; Li S; Engelen JJ; Bijlsma EK; Warburton PE
Prenat Diagn; 2003 Mar; 23(3):215-20. PubMed ID: 12627422
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Class II neocentromeres: a putative common neocentromere site in band 4q21.2.
Warburton PC; Barwell J; Splitt M; Maxwell D; Bint S; Ogilvie CM
Eur J Hum Genet; 2003 Oct; 11(10):749-53. PubMed ID: 14512964
[TBL] [Abstract][Full Text] [Related]
9. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
[TBL] [Abstract][Full Text] [Related]
10. A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines.
Gimelli G; Giorda R; Beri S; Gimelli S; Zuffardi O
Eur J Med Genet; 2007; 50(4):264-73. PubMed ID: 17567547
[TBL] [Abstract][Full Text] [Related]
11. Neocentromere formation in a stable ring 1p32-p36.1 chromosome.
Slater HR; Nouri S; Earle E; Lo AW; Hale LG; Choo KH
J Med Genet; 1999 Dec; 36(12):914-8. PubMed ID: 10593999
[TBL] [Abstract][Full Text] [Related]
12. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
[TBL] [Abstract][Full Text] [Related]
13. A small supernumerary marker chromosome, derived from chromosome 22, possibly associated with repeated spontaneous abortions.
Balkan M; Isi H; Gedik A; Erdemoğlu M; Budak T
Genet Mol Res; 2010 Aug; 9(3):1683-9. PubMed ID: 20799165
[TBL] [Abstract][Full Text] [Related]
14. Another small supernumerary marker chromosome (sSMC) derived from chromosome 2: towards a genotype/phenotype correlation.
Mrasek K; Starke H; Liehr T
J Histochem Cytochem; 2005 Mar; 53(3):367-70. PubMed ID: 15750022
[TBL] [Abstract][Full Text] [Related]
15. Interstitial deletion of the short arm of chromosome 6 as a new cytogenetic marker of T-cell lymphoma.
Maseki N; Kaneko Y; Sakurai M
Jpn J Cancer Res; 1986 Apr; 77(4):334-7. PubMed ID: 3084423
[TBL] [Abstract][Full Text] [Related]
16. Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.
Velissariou V; Sismani C; Christopoulou S; Kaminopetros P; Hatzaki A; Evangelidou P; Koumbaris G; Bartsocas CS; Stylianidou G; Skordis N; Diakoumakos A; Patsalis PC
Eur J Med Genet; 2007; 50(4):291-300. PubMed ID: 17584536
[TBL] [Abstract][Full Text] [Related]
17. Regional deletion and amplification on chromosome 6 in a uveal melanoma case without abnormalities on chromosomes 1p, 3 and 8.
van Gils W; Kilic E; Brüggenwirth HT; Vaarwater J; Verbiest MM; Beverloo B; van Til-Berg ME; Paridaens D; Luyten GP; de Klein A
Melanoma Res; 2008 Feb; 18(1):10-5. PubMed ID: 18227702
[TBL] [Abstract][Full Text] [Related]
18. Identification, characterization and clinical implications of two markers detected at prenatal diagnosis.
Leite RP; Souto M; Carvalho B; Martins M; Chaves R; Morais A; Guedes-Pinto H; Wienberg J; Ribeiro E
Prenat Diagn; 2006 Oct; 26(10):920-4. PubMed ID: 16845683
[TBL] [Abstract][Full Text] [Related]
19. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p.
Gawlik-Kuklinska K; Wierzba J; Wozniak A; Iliszko M; Debiec-Rychter M; Dubaniewicz-Wybieralska M; Limon J
Eur J Med Genet; 2008; 51(2):165-71. PubMed ID: 18243084
[TBL] [Abstract][Full Text] [Related]
20. [Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics].
Douet-Guilbert N; Basinko A; Le Bris MJ; Herry A; Morel F; De Braekeleer M
Pathol Biol (Paris); 2008 Sep; 56(6):362-7. PubMed ID: 18456432
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
