ArticleBMC medical genomics2021
A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes.
Rosaria Nardello et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
7 papers cite it
this papercites it
ArticleBMC medical genomics2021
Rosaria Nardello et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.