Identification of Diagnostic Variants in FGFR2 and NPR2 Genes in a Chinese Family Affected by Crouzon Syndrome and Acromesomelic Dysplasia, Type Maroteaux.
Zhu J, Meng R, Zhao H, Cai L, Wen X, Zeng W, Luo Y, Qi H. DNA Cell Biol. 2022 Nov; 41(11):996-1006. Epub 2022 Nov 2.