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Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndrome.
Higashimoto K, Nakabayashi K, Yatsuki H, Yoshinaga H, Jozaki K, Okada J, Watanabe Y, Aoki A, Shiozaki A, Saito S, Koide K, Mukai T, Hata K, Soejima H. Higashimoto K, et al. Among authors: koide k. Am J Med Genet A. 2012 Jul;158A(7):1670-5. doi: 10.1002/ajmg.a.35335. Epub 2012 May 10. Am J Med Genet A. 2012. PMID: 22577095
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome.
Higashimoto K, Maeda T, Okada J, Ohtsuka Y, Sasaki K, Hirose A, Nomiyama M, Takayanagi T, Fukuzawa R, Yatsuki H, Koide K, Nishioka K, Joh K, Watanabe Y, Yoshiura K, Soejima H. Higashimoto K, et al. Among authors: koide k. Eur J Hum Genet. 2013 Nov;21(11):1316-9. doi: 10.1038/ejhg.2013.45. Epub 2013 Mar 13. Eur J Hum Genet. 2013. PMID: 23486540 Free PMC article.
[Renal biopsy findings and pregnancy].
Abe S, Amagasaki Y, Konishi K, Iyori S, Kato E, Hirata K, Sakai O, Kitajima T, Ueda N, Koide K, Nagase M, Sakaguchi H. Abe S, et al. Among authors: koide k. Nihon Jinzo Gakkai Shi. 1982 Mar;24(3):275-84. Nihon Jinzo Gakkai Shi. 1982. PMID: 7120692 Japanese. No abstract available.
411 results