Literature DB >> 18978663

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

Murat Kadri Erdoğan1, Gülen Eda Utine, Yasemin Alanay, Dilek Aktaş.   

Abstract

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Mesh：

Year:  2008        PMID： 18978663     DOI： 10.1097/MCD.0b013e3283079e7c

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  3 in total

1.  A case of 22q11.2 deletion syndrome with Peters anomaly, congenital glaucoma, and heterozygous mutation in CYP1B1.

Authors:  Linda M Reis; Rebecca C Tyler; Roberto Zori; Jennifer Burgess; Jennifer Mueller; Elena V Semina
Journal:  Ophthalmic Genet       Date:  2013-09-11       Impact factor: 1.803

2.  Sclerocornea in a patient with van den Ende-Gupta syndrome homozygous for a SCARF2 microdeletion.

Authors:  Michele P Migliavacca; Nara L M Sobreira; Graziela P M Antonialli; Mariana M Oliveira; Maria Isabel S A Melaragno; Ingele Casteels; Thomy de Ravel; Decio Brunoni; David Valle; Ana Beatriz A Perez
Journal:  Am J Med Genet A       Date:  2014-01-29       Impact factor: 2.802

Review 3.  Chromosome abnormalities and the genetics of congenital corneal opacification.

Authors:  A Mataftsi; L Islam; D Kelberman; J C Sowden; K K Nischal
Journal:  Mol Vis       Date:  2011-06-17       Impact factor: 2.367
  3 in total

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