POGZ

Publications

Dentici ML et al. Expanding the phenotypic spectrum of truncating POGZ mutations: Association with CNS malformations, skeletal abnormalities, and distinctive facial dysmorphism. Am J Med Genet A. 2017;173(7):1965-1969. PMID: 28480548.

Stessman HAF et al. Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders. Am J Hum Genet. 2016;98(3):541-552. PMID: 26942287.

White J et al. POGZ truncating alleles cause syndromic intellectual disability. Genome Med. 2016; 8(1):3. PMID: 26739615.

Ye Y et al. De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly. Cold Spring Harb Mol Case Stud. 2015;1(1). PMID: 27148570.