TY  - GEN
AU  - Grønborg,Sabine
AU  - Kjaergaard,Susanne
AU  - Hove,Hanne
AU  - Larsen,Vibeke André
AU  - Kirchhoff,Maria
TI  - Monozygotic twins with a de novo 0.32 Mb 16q24.3 deletion, including TUBB3 presenting with developmental delay and mild facial dysmorphism but without overt brain malformation
SN  - 1552-4833
PY  - 2016///0829
KW  - Base Pairing
KW  - genetics
KW  - Brain
KW  - abnormalities
KW  - Chromosomes, Human, Pair 16
KW  - Comparative Genomic Hybridization
KW  - Developmental Disabilities
KW  - Facies
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Magnetic Resonance Imaging
KW  - Sequence Deletion
KW  - Tubulin
KW  - Twins, Monozygotic
N1  - Publication Type: Case Reports; Journal Article; Twin Study
UR  - https://doi.org/10.1002/ajmg.a.37227
ER  -