Novel 4.18 Mb deletion resulting in 2q37 microdeletion syndrome combined with PTH resistance found in one Chinese patient
Article in Endocrine (February 2024)
The most recent citing publications are shown below. View all 4 publications that cite this research output on Dimensions.
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly
Article in Journal of Bone and Mineral Research (December 2020)
Shortened Fingers and Toes: GNAS Abnormalities are Not the Only Cause
Article in Experimental and Clinical Endocrinology & Diabetes (December 2019)