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The Journal of Obstetrics and Gynaecology Research|February 18, 2026
Co-Occurrence of Osteogenesis Imperfecta Type III and Chronic Abruption-Oligohydramnios Sequence: A Case Report Suggesting a Possible Role of Type I Collagen FragilityAyumi Okuyama, Tatsuya Izdebski, Minako Goto, et al.
The Journal of Veterinary Medical Science|March 6, 2009
Systemic candidiasis and mesenteric mast cell tumor with multiple metastases in a dogKazuya Matsuda, Kanako Sakaguchi, Shintaro Kobayashi, et al.
Case Reports in Pediatrics|February 23, 2026
Kawasaki Disease in a Child With Trisomy 18 Treated With Initial Combination Therapy, Including CyclosporineYasuyuki Sahara, Naomi Yagi, Yoshitaka Watanabe, et al.
Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc|May 11, 2010
Flow cytometric analysis of peripheral blood and tumor-infiltrating regulatory T cells in dogs with oral malignant melanomaMakiko Tominaga, Yutaka Horiuchi, Mika Ichikawa, et al.
Human Genome Variation|October 25, 2019
Diamond-Blackfan anemia caused by chromosome 1p22 deletion encompassing <i>RPL5</i>Makiko Tominaga, Satoshi Hamanoue, Hiroaki Goto, et al.
Microbiology and Immunology|August 8, 2009
Increase of regulatory T cells in the peripheral blood of dogs with metastatic tumorsYutaka Horiuchi, Makiko Tominaga, Mika Ichikawa, et al.
Molecular Syndromology|May 20, 2021
A Recurrent Variant in <i>POLR1B</i>, c.3007C>T; p.Arg1003Cys, Associated with Atresia of the External Canal and Microtia in Treacher Collins Syndrome Type 4Yumi Enomoto, Yoshinori Tsurusaki, Makiko Tominaga, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
De novo duplication of 17p13.1-p13.2 in a patient with intellectual disability and obesityYukiko Kuroda, Ikuko Ohashi, Makiko Tominaga, et al.
Human Genome Variation|April 6, 2026
Clinical features of syndromic microphthalmia in two novel RARB variantsYoshito Koyanagi, Hazuki Morikawa-Anzai, Tomoyo Yoshida, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girlKeisuke Enomoto, Yasuhiro Kishitani, Makiko Tominaga, et al.
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