149 related articles for article (PubMed ID: 11170089)
1. Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromere.
Morrissette JD; Celle L; Owens NL; Shields CL; Zackai EH; Spinner NB
Am J Med Genet; 2001 Feb; 99(1):21-8. PubMed ID: 11170089
[TBL] [Abstract][Full Text] [Related]
2. Interstitial deletion of 13q and a 13;X chromosome translocation results in partial trisomy 13 and bilateral retinoblastoma.
Dries D; Baca K; Truss L; Dobin S
Ophthalmic Genet; 2003 Sep; 24(3):175-80. PubMed ID: 12868036
[TBL] [Abstract][Full Text] [Related]
3. Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.
Warburton PE; Dolled M; Mahmood R; Alonso A; Li S; Naritomi K; Tohma T; Nagai T; Hasegawa T; Ohashi H; Govaerts LC; Eussen BH; Van Hemel JO; Lozzio C; Schwartz S; Dowhanick-Morrissette JJ; Spinner NB; Rivera H; Crolla JA; Yu C; Warburton D
Am J Hum Genet; 2000 Jun; 66(6):1794-806. PubMed ID: 10777715
[TBL] [Abstract][Full Text] [Related]
4. Neocentromere at 13q32 in one of two stable markers derived from a 13q21 break.
Rivera H; Vasquez AI; García-Cruz D; Crolla JA
Am J Med Genet; 1999 Aug; 85(4):385-8. PubMed ID: 10398265
[TBL] [Abstract][Full Text] [Related]
5. Karyotyping in retinoblastoma--a statistical approach.
Joseph B; Paul PG; Elamparithi A; Roy J; Vidhya A; Shanmugam MP; Kumaramanickavel G
Asian Pac J Cancer Prev; 2005; 6(4):468-71. PubMed ID: 16435993
[TBL] [Abstract][Full Text] [Related]
6. Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
Tonnies H; Gerlach A; Heineking B; Starke H; Neitzel H; Neumann LM
Cytogenet Genome Res; 2006; 114(3-4):325-9. PubMed ID: 16954674
[TBL] [Abstract][Full Text] [Related]
7. Class II Analphoid Chromosome in a Child with Aberrant Chromosome 7: A Rare Cytogenetic Association.
Kumar MJ; Kumar RA; Subhashree V; Jayasudha T; Hemagowri V; Koshy T; Gowrishankar K
Cytogenet Genome Res; 2015; 146(2):120-123. PubMed ID: 26226839
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. The importance of excluding 13q deletion mosaicism in the diagnosis of retinoblastoma associated with dysmorphic features.
Van Esch H; Aerssens P; Fryns JP
Genet Couns; 2005; 16(1):91-3. PubMed ID: 15844785
[No Abstract] [Full Text] [Related]
11. Small Supernumerary Ring Chromosome Derived from an Inverted Duplication of 13q11.2q14 in a Fetus with Coarctation of the Aorta.
Zeng J; Huang M; Lin J; Zhang X; Lan F
Cytogenet Genome Res; 2019; 158(4):199-204. PubMed ID: 31315112
[TBL] [Abstract][Full Text] [Related]
12. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
[TBL] [Abstract][Full Text] [Related]
13. Retinoblastoma and Hirschsprung disease with a 13q14 to 22 deletion.
Zaborowski AG; Kruse CH; Kavonic S; Pergorano RJ
J Pediatr Ophthalmol Strabismus; 2008; 45(6):366-7. PubMed ID: 19043949
[TBL] [Abstract][Full Text] [Related]
14. Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.
Amare Kadam PS; Ghule P; Jose J; Bamne M; Kurkure P; Banavali S; Sarin R; Advani S
Cancer Genet Cytogenet; 2004 Apr; 150(1):33-43. PubMed ID: 15041221
[TBL] [Abstract][Full Text] [Related]
15. Characterization by FISH of a t(5;13) in a patient with bilateral retinoblastoma.
Triviño E; Guitart M; Egozcue J; Coll MD
Cancer Genet Cytogenet; 1997 Jul; 96(1):23-5. PubMed ID: 9209465
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Discordant retinoblastoma in monozygotic twins due to deletion of 13q14.
Messina-Baas OM; Arroyo-Yllanes ME; Pérez-Pérez JF; González-Huerta LM; Cuevas-Covarrubias SA
Eur J Ophthalmol; 2014; 24(6):968-71. PubMed ID: 24557757
[TBL] [Abstract][Full Text] [Related]
18. Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
Li S; Malafiej P; Levy B; Mahmood R; Field M; Hughes T; Lockhart LH; Wu Z; Huang M; Hirschhorn K; Velagaleti GV; Daniel A; Warburton PE
Am J Med Genet; 2002 Jul; 110(3):258-67. PubMed ID: 12116235
[TBL] [Abstract][Full Text] [Related]
19. Molecular evidence that the esterase-D gene lies proximal to the retinoblastoma susceptibility locus in chromosome region 13q14.
Mitchell CD; Cowell JK
Hum Genet; 1988 Dec; 81(1):57-60. PubMed ID: 3198126
[TBL] [Abstract][Full Text] [Related]
20. Retinoblastoma and deletion of the long arm of chromosome 13: an underestimated diagnosis?
Brichard B; Chantrain C; Gala JL; Sibille C; Vermylen C; De Potter P
Pediatr Blood Cancer; 2008 Mar; 50(3):694-6. PubMed ID: 16856159
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
