Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Enrique Sáinz González"'
Autor:
Juan Pablo Meza-Espinoza, Enrique Sáinz González, Christian J. N. León-León, Eliakym Arámbula-Meraz, José Alfredo Contreras-Gutiérrez, Noemí García-Magallanes, Jesús Madueña-Molina, Fred Luque-Ortega, Salvador Cervín-Serrano, Verónica Judith Picos-Cárdenas
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Abstract Background Concomitant trisomy 2q3 and monosomy 4q3 have been rarely reported. Pure trisomy 2q3 has been associated with microcephaly, hypertelorism, low-set ears, micrognathia, visceral abnormalities, and growth retardation. Monosomy 4q3 in
Externí odkaz:
https://doaj.org/article/982862c5d1c441fab377338617081324
Autor:
Verónica Judith Picos-Cárdenas, Juan Pablo Meza-Espinoza, Salvador Cervín-Serrano, José Alfredo Contreras-Gutiérrez, Christian J. N. León-León, Enrique Sáinz González, Jesús Madueña-Molina, Noemí García-Magallanes, Eliakym Arámbula-Meraz, Fred Luque-Ortega
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Molecular Cytogenetics
Molecular Cytogenetics
Background Concomitant trisomy 2q3 and monosomy 4q3 have been rarely reported. Pure trisomy 2q3 has been associated with microcephaly, hypertelorism, low-set ears, micrognathia, visceral abnormalities, and growth retardation. Monosomy 4q3 includes a
Autor:
Rocio Ortiz-Lopez, Roberto Iván Avendaño-Gálvez, Azubel Ramírez-Velazco, Verónica Judith Picos-Cárdenas, Horacio Rivera, Carlos Córdova-Fletes, Eliakym Arámbula-Meraz, Enrique Sáinz-González
Publikováno v:
Journal of genetics. 93(3)
1Laboratorio de Citogenomica y Microarreglos, Departamento de Bioquimica y Medicina Molecular, Facultad de Medicina, Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon 64460, Mexico 2Unidad de Biologia Molecular, Genomica y Secuenciacion, Cent