Similar articles for PMID: 12746416

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1

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. Meins M, et al. J Med Genet. 2003 May;40(5):e62. doi: 10.1136/jmg.40.5.e62. J Med Genet. 2003. PMID: 12746416 Free PMC article. Review. No abstract available.

2

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. Karcaaltincaba D, et al. Genet Couns. 2010;21(1):19-24. Genet Couns. 2010. PMID: 20420025

3

Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.

Knoll JH, Asamoah A, Pletcher BA, Wagstaff J. Knoll JH, et al. Am J Med Genet. 1995 Jan 16;55(2):221-4. doi: 10.1002/ajmg.1320550214. Am J Med Genet. 1995. PMID: 7717422 Review.

4

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. Vaglio A, et al. Eur J Med Genet. 2008 Jul-Aug;51(4):332-42. doi: 10.1016/j.ejmg.2008.01.001. Epub 2008 Jan 25. Eur J Med Genet. 2008. PMID: 18316257

5

Unilateral Peters' anomaly in an infant with 22q11.2 deletion syndrome.

Erdoğan MK, Utine GE, Alanay Y, Aktaş D. Erdoğan MK, et al. Clin Dysmorphol. 2008 Oct;17(4):289-90. doi: 10.1097/MCD.0b013e3283079e7c. Clin Dysmorphol. 2008. PMID: 18978663 No abstract available.

6

Ophthalmic findings with partial trisomy (duplication) of the long arm of chromosome 7.

Coats DK, Paysse EA, Palmer CG, Plager DA. Coats DK, et al. Can J Ophthalmol. 1998 Oct;33(6):337-41. Can J Ophthalmol. 1998. PMID: 9818133 Review. No abstract available.

7

Interrupted aortic arch type B in A patient with cat eye syndrome.

Belangero SI, Bellucco FT, Cernach MC, Hacker AM, Emanuel BS, Melaragno MI. Belangero SI, et al. Arq Bras Cardiol. 2009 May;92(5):e29-31, e56-8. doi: 10.1590/s0066-782x2009000500016. Arq Bras Cardiol. 2009. PMID: 19629279 Free PMC article.

8

Ocular abnormalities in Patau syndrome (chromosome 13 trisomy syndrome).

Koole FD, Velzeboer CM, van der Harten JJ. Koole FD, et al. Ophthalmic Paediatr Genet. 1990 Mar;11(1):15-21. doi: 10.3109/13816819009012944. Ophthalmic Paediatr Genet. 1990. PMID: 2348978

9

Cat-eye syndrome with different marker chromosomes in a mother and daughter.

Ing PS, Lubinsky MS, Smith SD, Golden E, Sanger WG, Duncan AM. Ing PS, et al. Am J Med Genet. 1987 Mar;26(3):621-8. doi: 10.1002/ajmg.1320260317. Am J Med Genet. 1987. PMID: 3105314

10

Ocular findings in the chromosome 22q11.2 deletion syndrome.

Forbes BJ, Binenbaum G, Edmond JC, DeLarato N, McDonald-McGinn DM, Zackai EH. Forbes BJ, et al. J AAPOS. 2007 Apr;11(2):179-82. doi: 10.1016/j.jaapos.2006.08.006. Epub 2006 Nov 30. J AAPOS. 2007. PMID: 17140829

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