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Cited by in F6Publishing
For: Ma Y, Xu Z, Zhao J, Shen H. Novel compound heterozygous mutations of PCNT gene in MOPD type II with central precocious puberty. Gynecol Endocrinol 2021;37:190-2. [PMID: 33016782 DOI: 10.1080/09513590.2020.1827382] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Liu H, Tao N, Wang Y, Yang Y, He X, Zhang Y, Zhou Y, Liu X, Feng X, Sun M, Xu F, Su Y, Li L. A novel homozygous mutation of the PCNT gene in a Chinese patient with microcephalic osteodysplastic primordial dwarfism type II. Mol Genet Genomic Med 2021;:e1761. [PMID: 34331829 DOI: 10.1002/mgg3.1761] [Reference Citation Analysis]
2 Hettiarachchi D, Subasinghe SMV, Anandagoda GG, Panchal H, Lai PS, Dissanayake VHW. Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys. BMC Med Genomics 2022;15. [DOI: 10.1186/s12920-022-01226-8] [Reference Citation Analysis]