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Fertility preservation in a family with a novel NR5A1 mutation.
Yagi H, Takagi M, Kon M, Igarashi M, Fukami M, Hasegawa Y. Yagi H, et al. Among authors: kon m. Endocr J. 2015;62(3):289-95. doi: 10.1507/endocrj.EJ14-0340. Epub 2014 Dec 12. Endocr J. 2015. PMID: 25502990 Free article.
Molecular basis of non-syndromic hypospadias: systematic mutation screening and genome-wide copy-number analysis of 62 patients.
Kon M, Suzuki E, Dung VC, Hasegawa Y, Mitsui T, Muroya K, Ueoka K, Igarashi N, Nagasaki K, Oto Y, Hamajima T, Yoshino K, Igarashi M, Kato-Fukui Y, Nakabayashi K, Hayashi K, Hata K, Matsubara Y, Moriya K, Ogata T, Nonomura K, Fukami M. Kon M, et al. Hum Reprod. 2015 Mar;30(3):499-506. doi: 10.1093/humrep/deu364. Epub 2015 Jan 20. Hum Reprod. 2015. PMID: 25605705
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.
Shima H, Hayashi M, Tachibana T, Oshiro M, Amano N, Ishii T, Haruna H, Igarashi M, Kon M, Fukuzawa R, Tanaka Y, Fukami M, Hasegawa T, Narumi S. Shima H, et al. Among authors: kon m. PLoS One. 2018 Nov 7;13(11):e0206184. doi: 10.1371/journal.pone.0206184. eCollection 2018. PLoS One. 2018. PMID: 30403727 Free PMC article.
544 results