CHIN-JUI WUSu Y.-N.Lin T.-H.LI-HUI TSENGKUANG-HAN CHAO2020-02-172020-02-1720151028-4559https://scholars.lib.ntu.edu.tw/handle/123456789/459832[SDGs]SDG3oligonucleotide; DNA; autosomal dominant inheritance; chromosome 19; chromosome 7; chromosome deletion; comparative genomic hybridization; copy number variation; development; echography; ectrodactyly; fetus echography; genetic counseling; genetic heterogeneity; Letter; adult; case report; chromosome 17; chromosome 7; chromosome deletion; comparative genomic hybridization; differential diagnosis; embryology; fatality; female; Fetal Diseases; genetics; human; Limb Deformities, Congenital; newborn; pregnancy; pregnancy outcome; procedures; Adult; Chromosome Deletion; Chromosomes, Human, Pair 17; Chromosomes, Human, Pair 7; Comparative Genomic Hybridization; Diagnosis, Differential; DNA; Fatal Outcome; Female; Fetal Diseases; Humans; Infant, Newborn; Limb Deformities, Congenital; Pregnancy; Pregnancy Outcome; Ultrasonography, Prenataljournal article10.1016/j.tjog.2014.01.006256759312-s2.0-84922823364