検索結果 - Messina-Baas, Olga

Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis 著者: Messina-Baas, Olga, Cuevas-Covarrubias, Sergio A.

全文の入手 全文の入手 全文の入手

A Family with Craniofrontonasal Syndrome and a Mutation (p.G151S) in the EFNB1 Gene: Expanding the Phenotype 著者: Toral-López, Jaime, González-Huerta, Luz M., Messina Baas, Olga, Cuevas-Covarrubias, Sergio A.

全文の入手 全文の入手 全文の入手

Submicroscopic 11p13 deletion including the elongator acetyltransferase complex subunit 4 gene in a girl with language failure, intellectual disability and congenital malformations... 著者: Toral-Lopez, Jaime, Huerta, Luz María González, Messina-Baas, Olga, Cuevas-Covarrubias, Sergio A

全文の入手 全文の入手 全文の入手

Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent Cataract 著者: Messina-Baas, Olga, Gonzalez-Garay, Manuel L., González-Huerta, Luz M., Toral-López, Jaime, Cuevas-Covarrubias, Sergio A.

全文の入手 全文の入手 全文の入手

Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic Cardiomyopathy 著者: Martin-de Saro, Monica, Compean, Zyndia, Aguilar, Karina, González-Huerta, Luz María, Plaza-Benhumea, Lautaro, Messina-Baas, Olga, Cuevas-Covarrubiass, Sergio Alberto

全文の入手 全文の入手 全文の入手

Jacobsen Syndrome: Surgical Complications due to Unsuspected Diagnosis, the Importance of Molecular Studies in Patients with Craniosynostosis 著者: 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.

全文の入手 全文の入手 全文の入手