An intellectually disabled patient with the 5q14.3q15 microdeletion syndrome associated with an apparently de novo t(2;5)(q13;q14)
Toral-López, Jaime, Buentello-Volante, Beatriz, Balderas-Minor, Marta M., Amezcua-Herrera, Carmen, Valdes-Miranda, Juan M., González-Huerta, Luz Ma, Gudiño, Marco, Cuevas-Covarrubias, Sergio A., Zenteno, Juan Carlos
Published in American journal of medical genetics. Part A (01.04.2012)
Published in American journal of medical genetics. Part A (01.04.2012)
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A Novel 23.1 Mb Interstitial Deletion Involving 7q22.3q32.1 in a Girl with Short Stature, Motor Delay, and Craniofacial Dysmorphism
del Refugio Rivera-Vega, Maria, Gómez-del Angel, Luis A., Valdes-Miranda, Juan M., Pérez-Cabrera, Adrián, Gonzalez-Huerta, Luz M., Toral-López, Jaime, Cuevas-Covarrubias, Sergio
Published in Cytogenetic and genome research (01.01.2015)
Published in Cytogenetic and genome research (01.01.2015)
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Martín-De Saro, Mónica D., Valdés-Miranda, Juan M., Plaza-Benhumea, Lautaro, Pérez-Cabrera, Adrián, Gonzalez-Huerta, Luz M., Guevara-Yañez, Roberto, Cuevas-Covarrubias, Sergio A.
Published in Cytogenetic and genome research (01.01.2015)
Published in Cytogenetic and genome research (01.01.2015)
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Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis
Linares Chávez, Etzalli P., Toral López, Jaime, Valdés Miranda, Juan M., González Huerta, Luz M., Perez Cabrera, Adrian, del Refugio Rivera Vega, María, Messina Baas, Olga M., Cuevas-Covarrubias, Sergio A.
Published in Molecular syndromology (01.02.2016)
Published in Molecular syndromology (01.02.2016)
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