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American Journal of Medical Genetics. Part A|October 18, 2008
Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36Shoji Saito, Rie Kawamura, Tomoki Kosho, et al.American Journal of Medical Genetics. Part A|March 26, 2014
Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: a clinical report and review of literatureYoko Narumi, Sachiko Nishina, Motoharu Tokimitsu, et al.Hepatology (Baltimore, Md.)|September 24, 2004
Peroxisome proliferator-activated receptor alpha protects against alcohol-induced liver damageTamie Nakajima, Yuji Kamijo, Naoki Tanaka, et al.Human Genome Variation|May 26, 2018
Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qterHirokazu Morokawa, Motoko Kamiya, Keiko Wakui, et al.American Journal of Medical Genetics. Part A|March 13, 2012
Neurodevelopmental features in 2q23.1 microdeletion syndrome: report of a new patient with intractable seizures and review of literatureMitsuo Motobayashi, Akira Nishimura-Tadaki, Yuji Inaba, et al.Annals of Vascular Diseases|April 5, 2013
Prediction of limb salvage after therapeutic angiogenesis by autologous bone marrow cell implantation in patients with critical limb ischemiaShuhei Tara, Masaaki Miyamoto, Gen Takagi, et al.Journal of Human Genetics|March 20, 2010
Cerebral hemorrhage in Fabry's diseaseKatsuya Nakamura, Yoshiki Sekijima, Kimitoshi Nakamura, et al.American Journal of Medical Genetics. Part A|December 7, 2013
Surgical intervention for esophageal atresia in patients with trisomy 18Eriko Nishi, Shigeru Takamizawa, Kenji Iio, et al.Clinical Dysmorphology|December 1, 2007
De-novo balanced translocation between 7q31 and 10p14 in a girl with central precocious puberty, moderate mental retardation, and severe speech impairmentTomoki Kosho, Satoru Sakazume, Hiroshi Kawame, et al.Journal of Human Genetics|December 13, 2006
A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12Yoshihiro Onouchi, Mayumi Tamari, Atsushi Takahashi, et al.Pageof 13