Noncongenital juvenile-onset bilateral lamellar cataract in 1p36 deletion syndrome

Author:

Danese Carla,Pignatto Silvia,Lanzetta Paolo

Publisher

Elsevier BV

Subject

Ophthalmology,Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008

2. Monosomy 1p36 deletion syndrome;Gajecka;Am J Med Genet Part C Semin Med Genet,2007

3. Molecular characterization of a monosomy 1p36 presenting as an aicardi syndrome phenocopy;Bursztejn;Am J Med Genet Part A,2009

4. Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome;Heilstedt;Am J Hum Genet,2003

5. Non-classical 1p36 deletion in a patient with Duane retraction syndrome: Case report and literature review;Yokoyama;Mol Cytogenet [Internet],2020

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