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9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (2)
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Display all abstracts in classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia
Search within classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia24008 Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia
Ito YA; Footz TK; Berry FB; Mirzayans F; Yu M; Khan AO; Walter MA
Investigative Ophthalmology and Visual Science 2009; 50: 3573-3579
24202 Genotype/phenotype association in Indian congenital aniridia
Neethirajan G; Solomon A; Krishnadas SR; Vijayalakshmi P; Sundaresan P
Indian Journal of Pediatrics 2009; 76: 513-517
