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The International Journal of Cardiovascular Imaging|April 8, 2015
Patients with reduced heart rate response to adenosine infusion have low myocardial flow reserve in (13)N-ammonia PET studiesTakeshi Tomiyama, Shin-ichiro Kumita, Keiichi Ishihara, 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.International Heart Journal|March 31, 2022
Localization of Late Gadolinium Enhancement and Its Association with Ventricular Tachycardia in Patients with Cardiac SarcoidosisKenji Yodogawa, Yoshimitsu Fukushima, Masaki Tachi, et al.Rinsho Byori. the Japanese Journal of Clinical Pathology|March 16, 2012
[Case with intrauterine fetus death: interphase fluorescence in situ hybridization using buccal cells is useful for examining chromosomal abnormalities when placental villus not available]Yuka Takezawa, Tomoki Kosho, Kazuyuki Matsuda, et al.International Journal of Cancer|November 4, 2004
DHPLC is superior to SSCP in screening p53 mutations in esophageal cancer tissuesOsamu Yamanoshita, Takeo Kubota, Jun Hou, et al.Journal of Human Genetics|April 15, 2006
A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in NaganoTakako Ohata, Kunihiro Yoshida, Haruya Sakai, et al.Journal of Human Genetics|April 17, 2002
A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feetShinji Kondoh, Hirobumi Sugawara, Naoki Harada, et al.Brain & Development|July 19, 2005
Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndromeKenji Kurosawa, Hiroshi Kawame, Nobuhiko Okamoto, et al.The Journal of Pediatrics|April 18, 2006
Phenotypic spectrum of CHARGE syndrome with CHD7 mutationsMichihiko Aramaki, Toru Udaka, Rika Kosaki, et al.American Journal of Medical Genetics. Part A|February 13, 2013
Clinical consequences in truncating mutations in exon 34 of NOTCH2: report of six patients with Hajdu-Cheney syndrome and a patient with serpentine fibula polycystic kidney syndromeYoko Narumi, Byung-Joo Min, Kenji Shimizu, et al.Pageof 13