TY  - GEN
AU  - Poelmans,G
AU  - Engelen,J J M
AU  - Van Lent-Albrechts,J
AU  - Smeets,H J
AU  - Schoenmakers,E
AU  - Franke,B
AU  - Buitelaar,J K
AU  - Wuisman-Frerker,M
AU  - Erens,W
AU  - Steyaert,J
AU  - Schrander-Stumpel,C
TI  - Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion
SN  - 1552-485X
PY  - 2009///0310
KW  - Adolescent
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 21
KW  - Dyslexia
KW  - genetics
KW  - Female
KW  - Genetic Linkage
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Male
KW  - Neuropsychological Tests
KW  - Oligonucleotide Array Sequence Analysis
KW  - Pedigree
KW  - Polymorphism, Single Nucleotide
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.b.30787
ER  -