Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype–phenotype correlations

European Journal of Human Genetics, Published online: 01 January 2022; doi:10.1038/s41431-021-01012-7Singleton exome sequencing of 90 fetuses with ultrasound anomalies revealing novel disease-causing variants and genotype–phenotype correlations

Source: European Journal of Human Genetics - January 1, 2022 Category: Genetics & Stem Cells Authors: Mateja Smogavec Maria Gerykova Bujalkova Reinhard Lehner J ürgen Neesen Jana Behunova G ülen Yerlikaya-Schatten Theresa Reischer Reinhard Altmann Denisa Weis Hans-Christoph Duba Franco Laccone Source Type: research