120 related articles for article (PubMed ID: 15642837)
1. 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]
2. 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]
3. 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]
4. [Ophthalmological manifestations of 13q deletion syndrome: A case report].
Iferkhass S; Elhalouat N; Boui H; Aziz O; Adil B; Laktaoui A
J Fr Ophtalmol; 2019 May; 42(5):e219-e224. PubMed ID: 30955898
[No Abstract] [Full Text] [Related]
5. 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]
6. 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]
7. 13q deletion syndrome associated with retinoblastoma and clinical anophthalmos of the opposite eye.
Hadjistilianou T; Mastrangelo D; Mazzotta C; De Francesco S; Capretti C; Lorè C
Med Pediatr Oncol; 2002 Apr; 38(4):293-4. PubMed ID: 11920804
[No Abstract] [Full Text] [Related]
8. [Monosomy 13q syndrome].
Tsukino R; Sasaki M
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):329-31. PubMed ID: 11057249
[No Abstract] [Full Text] [Related]
9. New findings in the chromosome 13 long-arm deletion syndrome and retinoblastoma.
Weichselbaum RR; Zakov ZN; Albert DM; Friedman AH; Nove J; Little JB
Ophthalmology; 1979 Jun; 86(6):1191-201. PubMed ID: 118416
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Interstitial deletion of 13q14.13-q32.3 presenting with Arima syndrome and bilateral retinoblastoma.
Takahashi K; Oka A; Mizuguchi M; Saitoh M; Takita J; Sato A; Mimaki M; Kato M; Ogawa S; Igarashi T
Brain Dev; 2011 Apr; 33(4):353-6. PubMed ID: 20728296
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Bilateral microphthalmos with colobomatous orbital cyst and de-novo balanced translocation t(3;5).
Kurbasic M; Jones FV; Cook LN
Ophthalmic Genet; 2000 Dec; 21(4):239-42. PubMed ID: 11135495
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Deletion (13)(q13q14.3) with retinoblastoma: confirmation and extension of a recognisable pattern of clinical features in retinoblastoma patients with 13q deletion.
Motegi T; Ikeda K; Watanabe K; Yanagawa Y; Minoda K
J Med Genet; 1987 Nov; 24(11):696-7. PubMed ID: 3430545
[TBL] [Abstract][Full Text] [Related]
17. Ocular abnormalities in Patau syndrome (chromosome 13 trisomy syndrome).
Koole FD; Velzeboer CM; van der Harten JJ
Ophthalmic Paediatr Genet; 1990 Mar; 11(1):15-21. PubMed ID: 2348978
[TBL] [Abstract][Full Text] [Related]
18. Clinical report of microphthalmia and optic nerve coloboma associated with a de novo microdeletion of chromosome 16p11.2.
Bardakjian TM; Kwok S; Slavotinek AM; Schneider AS
Am J Med Genet A; 2010 Dec; 152A(12):3120-3. PubMed ID: 21082658
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Genetic studies in retinoblastoma].
Bosun I; Puiu M
Oftalmologia; 1998; 45(4):28-34. PubMed ID: 10418625
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]