
Systematic genotype–phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22–q23 deletions
<a href="https://news.google.com/rss/articles/CBMiX0FVX3lxTE04ZURRc3ZRak1WbjZqdUlKYnlGTFRjRHB2bnpWbjZhS3oxa3FsQVlWV2doUWJuNWJYY2xLOF92Q1ZiN0FiZGFiTlh5Vkt6bVZsTFZ6Z2ZHS2psMkdGdEc0?oc=5" target="_blank">Systematic genotype–phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22–q23 deletions</a>&nbsp;&nbsp;<font color="#6f6f6f">Nature</font>
