TY  - GEN
AU  - Bayat,Allan
AU  - Kirchhoff,Maria
AU  - Madsen,Camilla G
AU  - Roos,Laura
AU  - Kreiborg,Sven
TI  - Familial craniofacial abnormality and polymicrogyria associated with a microdeletion affecting the NFIA gene
SN  - 1473-5717
PY  - 2018///0827
KW  - Child
KW  - Chromosome Deletion
KW  - Chromosome Mapping
KW  - Craniofacial Abnormalities
KW  - diagnosis
KW  - Facies
KW  - Female
KW  - Genetic Association Studies
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Magnetic Resonance Imaging
KW  - NFI Transcription Factors
KW  - genetics
KW  - Pedigree
KW  - Polymicrogyria
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1097/MCD.0000000000000182
ER  -