1. A case of 46, XY disorders of sex development with congenital heart disease caused by a GATA4 variant. (6th July 2022) Authors: Shichiri, Yui; Kato, Yoshimi; Inagaki, Hidehito; Kato, Takema; Ishihara, Naoko; Miyata, Masafumi; Boda, Hiroko; Kojima, Arisa; Miyake, Misa; Kurahashi, Hiroki Journal: Congenital anomalies Issue: Volume 62:Number 5(2022) Page Start: 203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. DNA methylation accumulation in gastric mucosa adjacent to cancer after Helicobacter pylori eradication. Issue 1 (12th November 2018) Authors: Tahara, Sayumi; Tahara, Tomomitsu; Horiguchi, Noriyuki; Kato, Takema; Shinkai, Yasuko; Yamashita, Hiromi; Yamada, Hyuga; Kawamura, Tomohiko; Terada, Tsuyoshi; Okubo, Masaaki; Nagasaka, Mitsuo; Nakagawa, Yoshihito; Shibata, Tomoyuki; Yamada, Seiji; Urano, Makoto; Tsukamoto, Tetsuya; Kurahashi, Hir... Journal: International journal of cancer Issue: Volume 144:Issue 1(2019) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome. (2nd October 2019) Authors: Toshimitsu, Masatake; Nagaoka, Shinichi; Kobori, Shuusaku; Ogawa, Maki; Suzuki, Fumihiko; Kato, Takema; Miyai, Shunsuke; Kawamura, Rie; Inagaki, Hidehito; Kurahashi, Hiroki; Murotsuki, Jun Other Names: Hoesli Irene Academic Editor. Journal: Case reports in obstetrics and gynecology Issue: Volume 2019(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Impact of DPYD, DPYS, and UPB1 gene variations on severe drug‐related toxicity in patients with cancer. Issue 9 (20th July 2020) Authors: Yokoi, Katsuyuki; Nakajima, Yoko; Matsuoka, Hiroshi; Shinkai, Yasuko; Ishihara, Takuma; Maeda, Yasuhiro; Kato, Takema; Katsuno, Hidetoshi; Masumori, Koji; Kawada, Kenji; Yoshikawa, Tetsushi; Ito, Tetsuya; Kurahashi, Hiroki Journal: Cancer science Issue: Volume 111:Issue 9(2020) Page Start: 3359 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Increased levels of soluble corin in pre-eclampsia and fetal growth restriction. (December 2016) Authors: Miyazaki, Jun; Nishizawa, Haruki; Kambayashi, Asuka; Ito, Mayuko; Noda, Yoshiteru; Terasawa, Sumire; Kato, Takema; Miyamura, Hironori; Shiogama, Kazuya; Sekiya, Takao; Kurahashi, Hiroki; Fujii, Takuma Journal: Placenta Issue: Volume 48(2016:Dec.) Page Start: 20 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Intragenic duplication in the PHKD1 gene in autosomal recessive polycystic kidney disease. Issue 1 (December 2015) Authors: Miyazaki, Jun; Ito, Mayuko; Nishizawa, Haruki; Kato, Takema; Minami, Yukito; Inagaki, Hidehito; Ohye, Tamae; Miyata, Masafumi; Boda, Hiroko; Kiriyama, Yuka; Kuroda, Makoto; Sekiya, Takao; Kurahashi, Hiroki; Fujii, Takuma Journal: BMC medical genetics Issue: Volume 16:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Lethal persistent pulmonary hypertension of the newborn in Bohring–Opitz syndrome. Issue 5 (21st April 2018) Authors: Kibe, Masaya; Ibara, Satoshi; Inagaki, Hidehito; Kato, Takema; Kurahashi, Hiroki; Ikeda, Toshiro Journal: American journal of medical genetics Issue: Volume 176:Issue 5(2018) Page Start: 1245 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Molecular analysis of low‐level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti. Issue 12 (21st October 2020) Authors: Kawai, Miki; Kato, Takema; Tsutsumi, Makiko; Shinkai, Yasuko; Inagaki, Hidehito; Kurahashi, Hiroki Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 12(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Multiplex PCR in noninvasive prenatal diagnosis for FGFR3‐related disorders. (15th April 2018) Authors: Terasawa, Sumire; Kato, Asuka; Nishizawa, Haruki; Kato, Takema; Yoshizawa, Hikari; Noda, Yoshiteru; Miyazaki, Jun; Ito, Mayuko; Sekiya, Takao; Fujii, Takuma; Kurahashi, Hiroki Journal: Congenital anomalies Issue: Volume 59:Number 1(2019) Page Start: 4 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Novel mutation in the KITLG gene in familial progressive hyperpigmentation with or without hypopigmentation. Issue 6 (18th March 2020) Authors: Kato, Maki; Yagami, Akiko; Tsukamoto, Tetsuya; Shinkai, Yasuko; Kato, Takema; Kurahashi, Hiroki Journal: Journal of dermatology Issue: Volume 47:Issue 6(2020) Page Start: 669 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗