TY  - GEN
AU  - Chen,Chih-Ping
AU  - Lin,Chen-Ju
AU  - Chen,Yi-Yung
AU  - Wang,Liang-Kai
AU  - Chern,Schu-Rern
AU  - Wu,Peih-Shan
AU  - Su,Jun-Wei
AU  - Chen,Li-Feng
AU  - Town,Dai-Dyi
AU  - Pan,Chen-Wen
AU  - Wang,Wayseen
TI  - 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization
SN  - 1879-0038
PY  - 2013///1223
KW  - Adult
KW  - Chromosome Deletion
KW  - Chromosome Duplication
KW  - Chromosomes, Human, Pair 3
KW  - Chromosomes, Human, Pair 9
KW  - Claudin-1
KW  - genetics
KW  - Claudins
KW  - Comparative Genomic Hybridization
KW  - methods
KW  - Face
KW  - abnormalities
KW  - Female
KW  - Heart Septal Defects, Ventricular
KW  - Hernia, Umbilical
KW  - Histone-Lysine N-Methyltransferase
KW  - Humans
KW  - Nuchal Translucency Measurement
KW  - Pregnancy
KW  - Pregnancy Trimester, First
KW  - Prenatal Diagnosis
KW  - Receptor, EphB3
KW  - Trisomy
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
UR  - https://doi.org/10.1016/j.gene.2013.09.025
ER  -