Associated Papers
CDKN1C gene mutation causing familial Silver-Russell syndrome: A case report and review of literature.
Li J et al.
World Journal of Clinical Cases, 2023
Analysis of CDKN1C in fetal growth restriction and pregnancy loss.
Suntharalingham JP et al.
F1000research, 2019
A novel variant in CDKN1C is associated with intrauterine growth restriction, short stature, and early-adulthood-onset diabetes.
Kerns SL et al.
The Journal of Clinical Endocrinology and Metabolism, 2014
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