Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology (Human Genetics and Genomics Advances (2022) 3(3), (S2666247722000185), (10.1016/j.xhgg.2022.100102))

University of Washington Center for Mendelian Genomics

Research output: Contribution to journalComment/debatepeer-review

1 Scopus citations

Fingerprint

Dive into the research topics of 'Erratum: Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology (Human Genetics and Genomics Advances (2022) 3(3), (S2666247722000185), (10.1016/j.xhgg.2022.100102))'. Together they form a unique fingerprint.

Medicine & Life Sciences