Publications by authors named "Jayson D Rodriguez"

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Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith-Magenis syndrome.
Gustavo H Vieira, Jayson D Rodriguez, Paulina Carmona-Mora, Lei Cao, Bruno F Gamba

Eur J Hum Genet· February 2012

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Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome.
Gustavo H Vieira, Jayson D Rodriguez, Raquel Boy, Isaias Soares de Paiva, Barbara R DuPont

Am J Med Genet A· May 2011

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Intellectual disability, midface hypoplasia, facial hypotonia, and Alport syndrome are associated with a deletion in Xq22.3.
Jayson D Rodriguez, Shambhu S Bhat, Ilaria Meloni, Sydney Ladd, Nancy D Leslie

Am J Med Genet A· March 2010

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