Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand-foot malformation. Role of EPS15L1 in pathogenesis

Hsueh Y.-L.SHIN-YU LINLin H.-Y.CHIEN-NAN LEEJIN-CHUNG SHIH2021-02-042021-02-0420151028-4559https://www.scopus.com/inward/record.uri?eid=2-s2.0-84941803403&doi=10.1016%2fj.tjog.2014.12.009&partnerID=40&md5=ae505d59854ccf83099be01035d11f68https://scholars.lib.ntu.edu.tw/handle/123456789/548106[SDGs]SDG2[SDGs]SDG3protein; protein eps15l1; unclassified drug; abortion; adult; Article; case report; chromosome 19p; chromosome 7p; comparative genomic hybridization; ectrodactyly; female; fetus; gene sequence; genetic association; gestational age; human; interstitial chromosome deletion; pathogenesis; patient counseling; phenotype; prognosis; second trimester pregnancy; amniocentesis; chromosome 7; chromosome deletion; comparative genomic hybridization; echography; fetus echography; genetics; limb malformation; pregnancy; procedures; rare disease; therapeutic abortion; Abortion, Therapeutic; Amniocentesis; Chromosome Deletion; Chromosomes, Human, Pair 7; Comparative Genomic Hybridization; Female; Humans; Limb Deformities, Congenital; Pregnancy; Pregnancy Trimester, Second; Rare Diseases; Ultrasonography, PrenatalArray comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand-foot malformation. Role of EPS15L1 in pathogenesisjournal article10.1016/j.tjog.2014.12.009263840722-s2.0-84941803403