Robert A Cucci - JoVE Visualize

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American Journal of Medical Genetics. Part A|December 18, 2003

Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutationsSai Prasad, Karen A Kölln, Robert A Cucci, et al.

Human Mutation|May 18, 2004

Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequencesEugene H Chang, Maithilee Menezes, Nicole C Meyer, et al.

Human Mutation|April 23, 2002

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing lossHossein Najmabadi, Robert A Cucci, Solmaz Sahebjam, et al.

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Showing results (1-10 of 3) with videos related to

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American Journal of Medical Genetics. Part A|December 18, 2003

Pendred syndrome and DFNB4-mutation screening of SLC26A4 by denaturing high-performance liquid chromatography and the identification of eleven novel mutationsSai Prasad, Karen A Kölln, Robert A Cucci, et al.

Human Mutation|May 18, 2004

Branchio-oto-renal syndrome: the mutation spectrum in EYA1 and its phenotypic consequencesEugene H Chang, Maithilee Menezes, Nicole C Meyer, et al.

Human Mutation|April 23, 2002

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing lossHossein Najmabadi, Robert A Cucci, Solmaz Sahebjam, et al.

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