TY  - GEN
AU  - Gazou,Anastasia
AU  - Riess,Angelika
AU  - Grasshoff,Ute
AU  - Schäferhoff,Karin
AU  - Bonin,Michael
AU  - Jauch,Anna
AU  - Riess,Olaf
AU  - Tzschach,Andreas
TI  - Xq22.3-q23 deletion including ACSL4 in a patient with intellectual disability
SN  - 1552-4833
PY  - 2013///0909
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Child
KW  - Chromosome Deletion
KW  - Chromosomes, Human, X
KW  - Coenzyme A Ligases
KW  - genetics
KW  - Facies
KW  - Gene Deletion
KW  - Genome-Wide Association Study
KW  - Genotype
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Intellectual Disability
KW  - Male
KW  - Phenotype
KW  - Polymorphism, Single Nucleotide
KW  - Long-Chain-Fatty-Acid-CoA Ligase
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1002/ajmg.a.35778
ER  -