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Clinical and Experimental Nephrology|March 13, 2016
Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencingTomohiko Yamamura, Naoya Morisada, Kandai Nozu, et al.
The Journal of International Medical Research|March 9, 2018
Clinical features predicting group A streptococcal pharyngitis in a Japanese paediatric primary emergency medical centreMasahiro Nishiyama, Ichiro Morioka, Mariko Taniguchi-Ikeda, et al.
Human Genome Variation|April 16, 2016
A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomyXue J Fu, Naoya Morisada, Fusako Hashimoto, et al.
Journal of Human Genetics|April 11, 2025
Regulation of MCCC1 expression by a Parkinson's disease-associated intronic variant: implications for pathogenesisShunsaku Sogabe, Hiroko Nakano, Yusuke Ogasahara, et al.
Molecular Cytogenetics|December 6, 2014
Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocationDivya Mishra, Takema Kato, Hidehito Inagaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|July 14, 2017
Evaluation of BiliCare™ transcutaneous bilirubin device in Japanese newbornsKeiji Yamana, Ichiro Morioka, Daisuke Kurokawa, et al.
Brain & Development|June 6, 2017
Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophyTetsushi Yamamoto, Mariko Taniguchi-Ikeda, Hiroyuki Awano, et al.
Brain & Development|August 13, 2015
Extremely preterm infants small for gestational age are at risk for motor impairment at 3 years corrected ageTakeshi Kato, Tsurue Mandai, Sota Iwatani, et al.
Human Genetics|August 24, 2023
Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature spermTakeshi Sugimoto, Hidehito Inagaki, Tasuku Mariya, et al.
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