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Congenital Anomalies|March 14, 2013
Patient with terminal 9 Mb deletion of chromosome 9p: refining the critical region for 9p monosomy syndrome with trigonocephalyNorimasa Mitsui, Kenji Shimizu, Hiroshi Nishimoto, et al.
Fetal and Pediatric Pathology|May 13, 2026
Utility of Integrating Genome-Wide Postmortem Testing into Clinical Autopsy Practice in Pediatrics: A Retrospective, Single-Center StudyNoriko Watanabe, Kayoko Ichimura, Daiju Oba, et al.
Spine|December 17, 2020
The Association of Scoliosis and NSD1 Gene Deletion in Sotos Syndrome PatientsMasafumi Machida, Hiroyuki Katoh, Masayoshi Machida, et al.
American Journal of Medical Genetics|February 22, 2002
Patellar dislocation in Kabuki syndromeKenji Kurosawa, Hiroshi Kawame, Yukikatsu Ochiai, et al.
Congenital Anomalies|March 2, 2005
Deletion involving the TWIST locus and the HOXA cluster: a contiguous gene syndrome on 7p?Rika Kosaki, Masataka Higuchi, Norimasa Mitsui, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 28, 2007
Non-invasive magnetic resonance imaging-guided focused ultrasound treatment for uterine fibroids - early experienceYutaka Morita, Naoki Ito, Hiromi Hikida, et al.
American Journal of Medical Genetics. Part A|April 1, 2004
Mosaic supernumerary inv dup(15) chromosome with four copies of the P gene in a boy with pigmentary dysplasiaKeiko Akahoshi, Richard A Spritz, Kazuyoshi Fukai, et al.
Clinical Case Reports|May 24, 2021
Impact of ivabradine in decompensated heart failure due to cancer therapy-related cardiac dysfunctionYusuke Nakano, Hirohiko Ando, Wataru Suzuki, et al.
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