TY  - GEN
AU  - Hancarova,Miroslava
AU  - Vejvalkova,Sarka
AU  - Trkova,Marie
AU  - Drabova,Jana
AU  - Dleskova,Alzbeta
AU  - Vlckova,Marketa
AU  - Sedlacek,Zdenek
TI  - Identification of a patient with intellectual disability and de novo 3.7 Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p15
SN  - 1879-0038
PY  - 2013///0325
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 2
KW  - Gene Deletion
KW  - Gene Dosage
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Intellectual Disability
KW  - diagnosis
KW  - Karyotype
KW  - Male
KW  - Microcephaly
KW  - Phenotype
KW  - Polymorphism, Single Nucleotide
KW  - Syndrome
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.gene.2012.12.027
ER  -