TY  - JOUR
AU  - Benítez-Burraco, Antonio
AU  - Barcos-Martínez, Montserrat
AU  - Espejo-Portero, Isabel
AU  - Fernández-Urquiza, Maite
AU  - Torres-Ruiz Raul, Raúl
AU  - Rodriguez Perales, Sandra
AU  - Jiménez-Romero, Ma Salud
PY  - 2018
DO  - 10.3389/fped.2018.00163
SN  - 2296-2360
UR  - http://hdl.handle.net/20.500.12105/8382
AB  - The chromosome 1q21.1 duplication syndrome (OMIM# 612475) is characterized by head anomalies, mild facial dysmorphisms, and cognitive problems, including autistic features, mental retardation, developmental delay, and learning disabilities. Speech and...
LA  - eng
PB  - Frontiers Media
KW  - CDH1L
KW  - ROBO1
KW  - Chromosome 1q21.1 duplication syndrome
KW  - Cognitive delay
KW  - Language deficits
KW  - Speech problems
TI  - Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome
TY  - journal article
ER  -