ERIC KAO to Female
This is a "connection" page, showing publications ERIC KAO has written about Female.
Connection Strength
0.056
-
MED12 Loss-of-Function Variants as a Cause of Congenital Diaphragmatic Hernia in Females With Hardikar Syndrome and Nonspecific Intellectual Disability. Am J Med Genet A. 2025 Jan; 197(1):e63868.
Score: 0.033
-
Loss of the maternal effect gene NLRP2 impairs embryonic and extra-embryonic development, revealing a novel genetic cause of congenital anomalies?. Biol Reprod. 2026 Apr 13; 114(4):1469-1485.
Score: 0.009
-
Clinicopathologic and Molecular Genetic Features of Spindle Cell Rhabdomyosarcoma Harboring ZFP64::NCOA2/3 Fusions: A Series of 14 Cases. Mod Pathol. 2025 Dec; 38(12):100906.
Score: 0.009
-
Dysregulation of nuclear receptor COUP-TFII impairs skeletal muscle development. Sci Rep. 2017 06 09; 7(1):3136.
Score: 0.005