A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies - Pode-Shakked, Ben; Barel, Ortal; Singer, Amihood; Regev, Miriam; Poran, Hana; Eliyahu, Aviva; Finezilber, Yael; Segev, Meirav; Berkenstadt, Michal; Yonath, Hagith; Reznik-Wolf, Haike; Gazit, Yael; et al. (Scientific reports, 2021)
Keywords: 631/208/1516; 692/4017; 692/617/375/366; Abnormalities, Multiple - diagnosis; Abnormalities, Multiple - economics; Abnormalities, Multiple - genetics; Adolescent; Adult; Autism; Child; Child, Preschool; Coexistence; Congenital defects; Congenital diseases; Cost-Benefit Analysis; Epilepsy; Feasibility Studies; Female; Financing, Government; Genetic Counseling - economics; Genetic Counseling - methods; Genetic Counseling - statistics & numerical data; Genetic Testing - economics; Genetic Testing - methods; Genetic Testing - statistics & numerical data; Humanities and Social Sciences; Humans; Infant; Infant, Newborn; Intellectual disabilities; Israel; Magnetic resonance imaging; Male; Maternal Age; Microencephaly; multidisciplinary; Neurodevelopmental disorders; Neurodevelopmental Disorders - diagnosis; Neurodevelopmental Disorders - economics; Neurodevelopmental Disorders - genetics; Neuroimaging; Paternal Age; Pregnancy; Premature birth; Prenatal Diagnosis - economics; Prenatal Diagnosis - methods; Program Evaluation; Retrospective Studies; Science; Science (multidisciplinary); Tertiary Care Centers - economics; Tertiary Care Centers - statistics & numerical data; Whole Exome Sequencing - economics; Whole Exome Sequencing - statistics & numerical data; Young Adult; Israel