133 related articles for article (PubMed ID: 9818133)
1. Ophthalmic findings with partial trisomy (duplication) of the long arm of chromosome 7.
Coats DK; Paysse EA; Palmer CG; Plager DA
Can J Ophthalmol; 1998 Oct; 33(6):337-41. PubMed ID: 9818133
[No Abstract] [Full Text] [Related]
2. Partial trisomy of chromosome 22 resulting from an interstitial duplication of 22q11.2 in a child with typical cat eye syndrome.
Meins M; Burfeind P; Motsch S; Trappe R; Bartmus D; Langer S; Speicher MR; Mühlendyck H; Bartels I; Zoll B
J Med Genet; 2003 May; 40(5):e62. PubMed ID: 12746416
[No Abstract] [Full Text] [Related]
3. [Ocular defects associated with a duplication of the distal part of the long arm of chromosome 1: a case report].
Le Goff L; Hadjadj E; Denis D
J Fr Ophtalmol; 2002 Apr; 25(4):388-92. PubMed ID: 12011743
[TBL] [Abstract][Full Text] [Related]
4. Ophthalmic findings in partial monosomy 4p (Wolf syndrome) in combination with partial trisomy 10p.
Seiberth V; Kachel W; Knorz MC; Liesenhoff H
Am J Ophthalmol; 1994 Mar; 117(3):411-3. PubMed ID: 8129026
[No Abstract] [Full Text] [Related]
5. Absence of a lateral rectus muscle associated with duplication of the chromosome segment 7q32----q34.
Keith CG; Webb GC; Rogers JG
J Med Genet; 1988 Feb; 25(2):122-5. PubMed ID: 3346885
[TBL] [Abstract][Full Text] [Related]
6. Partial trisomy due to a de novo duplication 22q11.1-22q13.1: a cat-eye syndrome variant with brain anomalies.
Karcaaltincaba D; Ceylaner S; Ceylaner G; Dalkilic S; Karli-Oguz K; Kandemir O
Genet Couns; 2010; 21(1):19-24. PubMed ID: 20420025
[TBL] [Abstract][Full Text] [Related]
7. Ocular pathology in trisomy 18. A histopathological report of three cases.
Velzeboer CM; van der Harten JJ; Koole FD
Ophthalmic Paediatr Genet; 1989 Dec; 10(4):263-9. PubMed ID: 2628818
[TBL] [Abstract][Full Text] [Related]
8. A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter-->22q12.1: clinical, cytogenetic and molecular observations.
Vaglio A; Milunsky A; Huang XL; Quadrelli A; Mechoso B; Maher TA; Quadrelli R
Eur J Med Genet; 2008; 51(4):332-42. PubMed ID: 18316257
[TBL] [Abstract][Full Text] [Related]
9. [Ocular signs of trisomy 13. General review].
Cordier J; Reny A; Kahn N
Adv Ophthalmol; 1971; 24(0):174-202. PubMed ID: 5006098
[No Abstract] [Full Text] [Related]
10. [Phenotype positioning on chromosomes in a patient with the syndrome of partial trisomy 7p21.2-->pter].
Liang DS; Wu LQ; Cai F; Xia K; Long ZG; Pan Q; Dai HP; Xia JH
Yi Chuan Xue Bao; 2005 Feb; 32(2):124-9. PubMed ID: 15759858
[TBL] [Abstract][Full Text] [Related]
11. Partial trisomy 15q: report of a patient and literature review.
Chandler K; Schrander-Stumpel CT; Engelen J; Theunissen P; Fryns JP
Genet Couns; 1997; 8(2):91-7. PubMed ID: 9219006
[TBL] [Abstract][Full Text] [Related]
12. [Molecular-cytogenetic identification of partial trisomy of a short arm of chromosome 8].
Zerova-Liubimova TE; Rigel M; Smul'skaia NA; Evseenkova EG; Gorovenko NG; Shintzel A
Tsitol Genet; 2004; 38(4):55-61. PubMed ID: 15715166
[TBL] [Abstract][Full Text] [Related]
13. Optic nerve hypoplasia associated with chromosome 9 inversion.
Cheung RT; Wong AM
Can J Ophthalmol; 2009 Oct; 44(5):610-1. PubMed ID: 19789607
[No Abstract] [Full Text] [Related]
14. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
[TBL] [Abstract][Full Text] [Related]
15. Ocular pathology of Trisomy 18.
Ginsberg J; Bove K; Nelson R; Englender GS
Ann Ophthalmol; 1971 Mar; 3(3):273-9. PubMed ID: 5005944
[No Abstract] [Full Text] [Related]
16. Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.
Kobrynski L; Chitayat D; Zahed L; McGregor D; Rochon L; Brownstein S; Vekemans M; Albert DL
Am J Med Genet; 1993 Apr; 46(1):68-71. PubMed ID: 8494034
[TBL] [Abstract][Full Text] [Related]
17. Prenatal detection of trisomy for the entire long arm of chromosome 7.
Ndah BV; Stead JA; Brancazio LR; Hummel M; Wenger SL
J Med Genet; 2000 Jul; 37(7):551-3. PubMed ID: 10970193
[No Abstract] [Full Text] [Related]
18. Aplasia of the optic nerve in two cases of partial trisomy 10q24-ter.
Pfeiffer RA; Jünemann A; Lorenz B; Sieber E
Clin Genet; 1995 Oct; 48(4):183-7. PubMed ID: 8591668
[TBL] [Abstract][Full Text] [Related]
19. Clinical, genetic and histopathologic findings in two siblings with muscle-eye-brain disease.
Zervos A; Hunt KE; Tong HQ; Avallone J; Morales J; Friedman N; Cohen BH; Clark B; Guo S; Gazda H; Beggs AH; Traboulsi EI
Eur J Ophthalmol; 2002; 12(4):253-61. PubMed ID: 12219993
[TBL] [Abstract][Full Text] [Related]
20. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
Schürmann M; Wethling H; Niemeyer ML; Schwinger E
Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]