Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study

• Main Authors: Li, Jianqiao (Author), Hojlo, Margaret A (Author), Chennuri, Sampath (Author), Gujral, Nitin (Author), Paterson, Heather L (Author), Shefchek, Kent A (Author), Genetti, Casie A (Author), Cohn, Emily L (Author), Sewalk, Kara C (Author), Garvey, Emily A (Author), Buttermore, Elizabeth D (Author), Anderson, Nickesha C (Author), Beggs, Alan H (Author), Agrawal, Pankaj B (Author), Brownstein, John S (Author), Haendel, Melissa A (Author), Holm, Ingrid A (Author), Gonzalez-Heydrich, Joseph (Author), Brownstein, Catherine A (Author)
• 格式: 图书
• 出版: JMIR Publications, 2021-03-01T00:00:00Z.
• 主题: article
• 在线阅读: Connect to this object online.

Background16p13.11 microduplication syndrome has a variable presentation and is characterized primarily by neurodevelopmental and physical phenotypes resulting from copy number variation at chromosome 16p13.11. Given its variability, there may be features that have not yet been reported. The goal of...