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Paper Details

Exome and RNA-Seq analyses of an incomplete penetrance variant in USP9X in female-specific syndromic intellectual disability.
Am J Med Genet A
1
2022
ID, MIM 300969, MRX99F, RNA, USP9X, USP9X gene, X chromosome, c.885, quad exome, syndromic ID, syndromic intellectual disability
Author NameAffiliation
Dong LiCenter for Applied Genomics, The Children's Hospital of Philadelphia
Michael E MarchCenter for Applied Genomics, The Children's Hospital of Philadelphia
Hakon HakonarsonCenter for Applied Genomics, The Children's Hospital of Philadelphia
Hakon HakonarsonThe Children's Hospital of Philadelphia
Hakon HakonarsonCenter for Applied Genomics, The Children's Hospital of Philadelphia
Hakon HakonarsonThe Children's Hospital of Philadelphia
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