Associated Papers
Identification of five novel BOR mutations in human EYA1 gene associated with branchio-oto-renal syndrome by a DHPLC-based assay.
Migliosi V et al.
Clinical Genetics, 2004
Branchio-oto-renal syndrome: identification of a novel mutation in the EYA1 gene.
Rodríguez-Soriano J et al.
Pediatric Nephrology (berlin, Germany), 2001
Mutations in the MECP2 gene in a cohort of girls with Rett syndrome.
Hampson K et al.
Journal of Medical Genetics, 2000
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