Robert A. Cucci

Pendred syndrome, DFNB4, andPDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations

Colleen A. Campbell, Robert A. Cucci, Sai Prasad et al. · Human Mutation · 2001 · 297 citations

Branchio-oto-renal syndrome: The mutation spectrum in<i>EYA1</i>and its phenotypic consequences

Eugene H. Chang, Maithilee Menezes, Nicole C. Meyer et al. · Human Mutation · 2004 · 221 citations

Urology, Genetic Testing, Mendelian Disorder +12

Genetic testing for hereditary hearing loss: Connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA)

Sai Prasad, Robert A. Cucci, Glenn E. Green et al. · Human Mutation · 2000 · 71 citations

Genetics, Pathology, Gjb2 Mutation +16

Pendred syndrome and DFNB4‐mutation screening of <i>SLC26A4</i> by denaturing high‐performance liquid chromatography and the identification of eleven novel mutations

Sai Prasad, Karen A. Kölln, Robert A. Cucci et al. · American Journal of Medical Genetics Part A · 2003 · 63 citations · Full text

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss

Hossein Najmabadi, Robert A. Cucci, Solmaz Sahebjam et al. · Human Mutation · 2002 · 52 citations · Full text