Williams–Beuren syndrome in Mexican patients confirmed by FISH and assessed by aCGH von Ramírez-Velazco, Azubel, Aguayo-Orozco, Thania Alejandra, Figuera, Luis, Rivera, Horacio, Jave-Suárez, Luis, Aguilar-Lemarroy, Adriana, Torres-Reyes, Luis A., Córdova-Fletes, Carlos, Barros-Núñez, Patricio, Delgadillo-Pérez, Saturnino, Dávalos-Rodríguez, Ingrid Patricia, García-Ortiz, José Elías, Domínguez, María G.

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Two further triple-X/rea(X) females in an inv(X)(p22q22) family von RIVERA, HORACIO, VÁSQUEZ-VELÁSQUEZ, ANA I., DOMÍNGUEZ-QUEZADA, MARIA G., RAMÍREZ-VELAZCO, AZUBEL

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22q11.2 deletion detected by in situ hybridization in 22/39 Mexican patients with velocardiofacial syndrome-like features von Ramírez-Velazco, Azubel, Rivera, Horacio, Vásquez-Velázquez, Ana Isabel, Aguayo-Orozco, Thania Alejandra, Delgadillo- Pérez, Saturnino, Domínguez, María Guadalupe

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Complex 9p rearrangement in an XY patient with ambiguous genitalia and features of both 9p duplication and deletion von Neira, Vivian Alejandra, Córdova-Fletes, Carlos, Grondin, Yohann, Ramirez-Velazco, Azubel, Figuera, Luis E., Ortíz-López, Rocío, Barbaro, Michela

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De novo dir dup/del of 18q characterized by SNP arrays and FISH in a girl child with mixed phenotypes von CÓRDOVA-FLETES, CARLOS, SÁINZ-GONZÁLEZ, ENRIQUE, AVENDAÑO-GÁLVEZ, ROBERTO IVÁN, RAMÍREZ-VELAZCO, AZUBEL, RIVERA, HORACIO, ORTIZ-LÓPEZ, ROCÍO, ARÁMBULA-MERAZ, ELIAKYM, PICOS-CÁRDENAS, VERÓNICA JUDITH

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22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features von Ramírez-Velazco, Azubel, Rivera, Horacio, Vásquez-Velázquez, Ana Isabel, Aguayo-Orozco, Thania Alejandra, Delgadillo-Pérez, Saturnino, Domínguez, Maria Guadalupe

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22q11.2 deletion detected by in situ hybridization in Mexican patients with velocardiofacial syndrome-like features von Ramírez Velazco, Azubel, Rivera, Horacio, Vásquez Velázquez, Ana Isabel, Aguayo Orozco, Thania Alejandra, Delgadillo Pérez, Saturnino, Domínguez, María Guadalupe

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Two further triple-X/rea family von RIVERA, HORACIO, VÁSQUEZ-VELÁSQUEZ, ANA I, DOMÍNGUEZ-QUEZADA, MARIA G, RAMÍREZ-VELAZCO, AZUBEL

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Deleción 22q11.2 detectada por hibridación in situ en pacientes mexicanos con características clínicas similares al síndrome velocardiofacial von Ramírez, Velazco Azubel, Rivera, Horacio, Vásquez, Velázquez Ana Isabel, Aguayo, Orozco Thania Alejandra, Delgadillo, Pérez Saturnino, Domínguez, Ma. Guadalupe

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