Literature DB >> 15642837

Variable expression of ophthalmological findings in the 13q deletion syndrome.

Peter J Lansink, Annette C Moll, Saskia M Imhof, Antoinette Y N Schouten-van Meeteren, S Theo Goverts.   

Abstract

Mesh：

Year:  2005        PMID： 15642837     DOI： 10.1001/archopht.123.1.127-c

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


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  2 in total

Review 1.  The contribution of associated congenital anomalies in understanding Hirschsprung's disease.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2006-03-04       Impact factor: 1.827

2.  Array comparative genomic hybridization analysis in patients with anophthalmia, microphthalmia, and coloboma.

Authors:  Gordana Raca; Craig A Jackson; Laimutis Kucinskas; Berta Warman; Joseph T C Shieh; Adele Schneider; Tanya M Bardakjian; Lisa A Schimmenti
Journal:  Genet Med       Date:  2011-05       Impact factor: 8.822
  2 in total

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