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Human Genome Variation|August 23, 2018
Late-onset ornithine transcarbamylase deficiency caused by a somatic mosaic mutationTomoko Lee, Maiko Misaki, Hideki Shimomura, et al.African Journal of Paediatric Surgery : AJPS|February 10, 2015
Unilateral pulmonary agenesis associated with oesophageal atresia and tracheoesophageal fistula: A case report with prenatal diagnosisGo Miyano, Keiichi Morita, Masakatsu Kaneshiro, et al.Journal of Vestibular Research : Equilibrium & Orientation|May 8, 2010
Proteomic analysis of the rat cerebellar flocculus during vestibular compensationMasahiko Fukasawa, Kazuki Okamoto, Manabu Nakamura, et al.Investigative Ophthalmology & Visual Science|December 24, 2003
Purification, molecular cloning, and expression of a novel growth-promoting factor for retinal pigment epithelial cells, REF-1/TFPI-2Yasuhiko Tanaka, Jun Utsumi, Mizuo Matsui, et al.Pediatric Surgery International|July 28, 2016
Risk factors and prevention for surgical intestinal disorders in extremely low birth weight infantsMasaya Yamoto, Yusuke Nakazawa, Koji Fukumoto, et al.Investigative Ophthalmology & Visual Science|January 27, 2005
Early-onset macular degeneration with drusen in a cynomolgus monkey (Macaca fascicularis) pedigree: exclusion of 13 candidate genes and lociShinsuke Umeda, Radha Ayyagari, Rando Allikmets, et al.Children (Basel, Switzerland)|January 21, 2022
Early Developmental Signs in Children with Autism Spectrum Disorder: Results from the Japan Environment and Children's StudyHideki Shimomura, Hideki Hasunuma, Sachi Tokunaga, et al.Circulation. Arrhythmia and Electrophysiology|December 10, 2009
Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in JapanHitoshi Horigome, Masami Nagashima, Naokata Sumitomo, et al.Pageof 5