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Compound heterozygosity of a de novo submicroscopic deletion and an inherited frameshift pathogenic variant in the PKHD1 gene in a fetus with bilaterally enlarged and echogenic kidneys, enlarged abdomen and oligohydramnios.
Sakyu T, Stover SR, Wang Y, Ward P, Gandhi M, Braun MC, Van den Veyver IB, Bi W. Sakyu T, et al. Clin Case Rep. 2023 Feb 23;11(2):e6692. doi: 10.1002/ccr3.6692. eCollection 2023 Feb. Clin Case Rep. 2023. PMID: 36846174 Free PMC article.
Runx2 in human breast carcinoma: its potential roles in cancer progression.
Onodera Y, Miki Y, Suzuki T, Takagi K, Akahira J, Sakyu T, Watanabe M, Inoue S, Ishida T, Ohuchi N, Sasano H. Onodera Y, et al. Among authors: sakyu t. Cancer Sci. 2010 Dec;101(12):2670-5. doi: 10.1111/j.1349-7006.2010.01742.x. Epub 2010 Oct 12. Cancer Sci. 2010. PMID: 20946121 Free article.