TY  - GEN
AU  - Tejada, María-Isabel
AU  - Glover, Guillermo
AU  - Martínez, Francisco
AU  - Guitart, Miriam
AU  - Diego-Otero, Yolanda de
AU  - Fernández-Carvajal, Isabel
AU  - Ramos, Feliciano J
AU  - Hernández-Chico, Concepción
AU  - Pintado, Elizabet
AU  - Rosell, Jordi
AU  - Calvo, María-Teresa
AU  - Ayuso, Carmen
AU  - Ramos-Arroyo, María-Antonia
AU  - Maortua, Hiart
AU  - Milà, Montserrat
PY  - 2014
DO  - 10.1155/2014/195793
UR  - http://hdl.handle.net/20.500.12105/17069
AB  - Fragile X syndrome is the most common inherited form of intellectual disability. Here we report on a study based on a collaborative registry, involving 12 Spanish centres, of molecular diagnostic tests in 1105 fragile X families comprising 5062...
LA  - eng
PB  - Hindawi
KW  - Alelos
KW  - Síndrome del cromosoma X frágil
KW  - Frecuencia génica
KW  - Pruebas genéticas
KW  - Sistema de registros
KW  - España
KW  - Adult
KW  - Alleles
KW  - Child
KW  - Child, Preschool
KW  - Female
KW  - Fragile X Syndrome
KW  - Gene Frequency
KW  - Genetic Testing
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Middle Aged
KW  - Registries
KW  - Spain
KW  - Adolescent
TI  - Molecular testing for fragile X: analysis of 5062 tests from 1105 fragile X families--performed in 12 clinical laboratories in Spain.
TY  - research article
ER  -