146 related articles for article (PubMed ID: 22505049)
1. 13q deletion syndrome and retinoblastoma in identical dichorionic diamniotic monozygotic twins.
De Francesco S; Galluzzi P; Del Longo A; Piozzi E; Renieri A; Menicacci C; Mari F; Munier F; Hadjistilianou T; Mastrangelo D
Eur J Ophthalmol; 2012; 22(5):857-60. PubMed ID: 22505049
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. PARTIAL TRISOMY 4p AND PARTIAL MONOSOMY 13q: CASE REPORT AND A LITERATURE REVIEW.
Puvabanditsin S; Herrera-Garcia G; Gengel N; Hussein K; February M; Mayne J; Mehta R
Genet Couns; 2016; 27(1):35-41. PubMed ID: 27192890
[TBL] [Abstract][Full Text] [Related]
5. Retinoblastoma in a patient with an X;13 translocation and facial abnormalities consistent with 13q-syndrome.
Laquis SJ; Rodriguez-Galindo C; Wilson MW; Fleming JC; Haik BG
Am J Ophthalmol; 2002 Feb; 133(2):285-7. PubMed ID: 11812445
[TBL] [Abstract][Full Text] [Related]
6. Brain abnormalities on MR imaging in patients with retinoblastoma.
Rodjan F; de Graaf P; Moll AC; Imhof SM; Verbeke JI; Sanchez E; Castelijns JA
AJNR Am J Neuroradiol; 2010 Sep; 31(8):1385-9. PubMed ID: 20413604
[TBL] [Abstract][Full Text] [Related]
7. [Retinoblastoma in monozygotic twins].
Procházková D; Konecná P; Cíhalová V; Hrstková H; Rehůrek J; Autrata R
Cesk Slov Oftalmol; 2003 Mar; 59(2):134-40. PubMed ID: 12825405
[TBL] [Abstract][Full Text] [Related]
8. Retinoblastoma and the 13q deletion syndrome.
Ganesh A; Kenue RK; Mitra S
J Pediatr Ophthalmol Strabismus; 2001; 38(4):247-50. PubMed ID: 11495315
[No Abstract] [Full Text] [Related]
9. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
10. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome.
Wilson GA; Devaux A; Aroichane M
Clin Exp Ophthalmol; 2004 Feb; 32(1):101-3. PubMed ID: 14746602
[TBL] [Abstract][Full Text] [Related]
11. Bilateral retinoblastoma, microphthalmia, and colobomas in the 13q deletion syndrome.
Schocket LS; Beaverson KL; Rollins IS; Abramson DH
Arch Ophthalmol; 2003 Jun; 121(6):916-7. PubMed ID: 12796275
[No Abstract] [Full Text] [Related]
12. Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions.
Mitter D; Ullmann R; Muradyan A; Klein-Hitpass L; Kanber D; Ounap K; Kaulisch M; Lohmann D
Eur J Hum Genet; 2011 Sep; 19(9):947-58. PubMed ID: 21505449
[TBL] [Abstract][Full Text] [Related]
13. Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.
Lillington DM; Kingston JE; Coen PG; Price E; Hungerford J; Domizio P; Young BD; Onadim Z
Genes Chromosomes Cancer; 2003 Feb; 36(2):121-8. PubMed ID: 12508240
[TBL] [Abstract][Full Text] [Related]
14. Retinoblastoma associated with chromosomal 13q14 deletion mosaicism.
Kivelä T; Tuppurainen K; Riikonen P; Vapalahti M
Ophthalmology; 2003 Oct; 110(10):1983-8. PubMed ID: 14522775
[TBL] [Abstract][Full Text] [Related]
15. Retinoblastoma and mental retardation microdeletion syndrome: clinical characterization and molecular dissection using array CGH.
Caselli R; Speciale C; Pescucci C; Uliana V; Sampieri K; Bruttini M; Longo I; De Francesco S; Pramparo T; Zuffardi O; Frezzotti R; Acquaviva A; Hadjistilianou T; Renieri A; Mari F
J Hum Genet; 2007; 52(6):535-542. PubMed ID: 17502991
[TBL] [Abstract][Full Text] [Related]
16. 25 Mb deletion of 13q13.3-->q21.31 in a patient without retinoblastoma.
Thienpont B; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):363-6. PubMed ID: 16179234
[No Abstract] [Full Text] [Related]
17. Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.
Goodship J; Cross I; Scambler P; Burn J
J Med Genet; 1995 Sep; 32(9):746-8. PubMed ID: 8544199
[TBL] [Abstract][Full Text] [Related]
18. Dysmorphic phenotype and neurological impairment in 22 retinoblastoma patients with constitutional cytogenetic 13q deletion.
Baud O; Cormier-Daire V; Lyonnet S; Desjardins L; Turleau C; Doz F
Clin Genet; 1999 Jun; 55(6):478-82. PubMed ID: 10450867
[TBL] [Abstract][Full Text] [Related]
19. [Identification of a novel deletion region in 3q29 microdeletion syndrome by oligonucleotide array comparative genomic hybridization].
Seo EJ; Jun KR; Yoo HW; Yoo HK; Lee JO
Korean J Lab Med; 2010 Feb; 30(1):70-5. PubMed ID: 20197726
[TBL] [Abstract][Full Text] [Related]
20. Variable expression of ophthalmological findings in the 13q deletion syndrome.
Lansink PJ; Moll AC; Imhof SM; Schouten-van Meeteren AY; Goverts ST
Arch Ophthalmol; 2005 Jan; 123(1):127-8; author reply 128. PubMed ID: 15642837
[No Abstract] [Full Text] [Related]
[Next] [New Search]