TY  - JOUR
AU  - Benitez-Burraco, Antonio
AU  - Barcos-Martinez, Montserrat
AU  - Espejo-Portero, Isabel
AU  - Fernandez-Urquiza, Maite
AU  - Torres-Ruiz, Raul
AU  - Rodriguez-Perales, Sandra
AU  - Jimenez-Romero, Ma Salud
PY  - 2018
DO  - 10.3389/fped.2018.00163
SN  - 2296-2360
UR  - http://hdl.handle.net/10668/12614
T2  - Frontiers in pediatrics
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  - en
PB  - Frontiers Research Foundation
KW  - CDH1L
KW  - ROBO1
KW  - Chromosome 1q21.1 duplication syndrome
KW  - Cognitive delay
KW  - Language deficits
KW  - Speech problems
KW  - Intellectual disability
KW  - Nerve tissue proteins
KW  - Autistic disorder
KW  - Comprehension
KW  - Receptors, immunologic
KW  - Dyslexia
KW  - Learning disabilities
KW  - Communication disorders
TI  - Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome.
TY  - research article
VL  - 6
ER  -