Publications by authors named "Sherly Pardo"

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Clinical Cancer Genetics Disparities among Latinos.
Marcia Cruz-Correa, Julyann Pérez-Mayoral, Julie Dutil, Miguel Echenique, Rafael Mosquera, Sherly Pardo

J Genet Couns· June 2017

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Hereditary cancer syndromes in Latino populations: genetic characterization and surveillance guidelines.
Marcia Cruz-Correa, Julyann Pérez-Mayoral, Julie Dutil, Miguel Echenique, Rafael Mosquera, Sherly Pardo

Hered Cancer Clin Pract· January 2017

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Prevalence and Genetic Profile of Duchene and Becker Muscular Dystrophy in Puerto Rico.
Edwardo Ramos, José G Conde, Rafael Arias Berrios, Sherly Pardo, Omar Gómez

J Neuromuscul Dis· May 2016

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Limb-Girdle Muscular Dystrophy Type 2A Resulting From c.C479G and c.G1818A Mutations in the Calpain-3 Gene.
Edwardo Ramos, Sherly Pardo, Manuel F Mas Rodríguez, John Vélez

J Clin Neuromuscul Dis· December 2015

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Myeloid Dysregulation in a Human Induced Pluripotent Stem Cell Model of PTPN11-Associated Juvenile Myelomonocytic Leukemia.
Sonia Mulero-Navarro, Ana Sevilla, Angel C Roman, Dung-Fang Lee, Sunita L D'Souza, Sherly Pardo

Cell Rep· October 2015

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Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome.
Marcia Cruz-Correa, Yaritza Diaz-Algorri, Julyann Pérez-Mayoral, Wasilah Suleiman-Suleiman, Maria del Mar Gonzalez-Pons, Sherly Pardo

Fam Cancer· September 2015

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RAF1 mutations in childhood-onset dilated cardiomyopathy.
Perundurai S Dhandapany, Md Abdur Razzaque, Uthiralingam Muthusami, Sreejith Kunnoth, Jonathan J Edwards, Sherly Pardo

Nat Genet· June 2014

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Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome.
Xonia Carvajal-Vergara, Ana Sevilla, Sunita L D'Souza, Yen-Sin Ang, Christoph Schaniel, Sherly Pardo

Nature· June 2010

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Multiple hemangiomas in a patient with a t(3q;4p) translocation: an infrequent association with Wolf-Hirschhorn syndrome.
Sherly Pardo, Netta Blitman, Bokyung Han, Ninette Cohen, Lisa Edelmann

Am J Med Genet A· January 2008

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An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism.
Lisa Edelmann, Aaron Prosnitz, Sherly Pardo, Jahnavi Bhatt, Ninette Cohen

J Med Genet· February 2007

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