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A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.
Isojima T, Doi K, Mitsui J, Oda Y, Tokuhiro E, Yasoda A, Yorifuji T, Horikawa R, Yoshimura J, Ishiura H, Morishita S, Tsuji S, Kitanaka S. Isojima T, et al. Among authors: yorifuji t. J Bone Miner Res. 2014 Apr;29(4):992-8. doi: 10.1002/jbmr.2091. J Bone Miner Res. 2014. PMID: 23996431 Free article.
Chromosome 6q24-related diabetes mellitus.
Yorifuji T, Higuchi S, Hosokawa Y, Kawakita R. Yorifuji T, et al. Clin Pediatr Endocrinol. 2018;27(2):59-65. doi: 10.1297/cpe.27.59. Epub 2018 Apr 13. Clin Pediatr Endocrinol. 2018. PMID: 29662264 Free PMC article.
Pregnancy outcome of Japanese patients with glucokinase-maturity-onset diabetes of the young.
Hosokawa Y, Higuchi S, Kawakita R, Hata I, Urakami T, Isojima T, Takasawa K, Matsubara Y, Mizuno H, Maruo Y, Matsui K, Aizu K, Jinno K, Araki S, Fujisawa Y, Osugi K, Tono C, Takeshima Y, Yorifuji T. Hosokawa Y, et al. Among authors: yorifuji t. J Diabetes Investig. 2019 Nov;10(6):1586-1589. doi: 10.1111/jdi.13046. Epub 2019 Apr 23. J Diabetes Investig. 2019. PMID: 30897270 Free PMC article.
487 results