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Surgery Today|November 7, 1999
An extremely large solitary primary paraganglioma of the lung: report of a caseT Saeki, T Akiba, K Joh, et al.
Scandinavian Journal of Rheumatology|December 20, 2007
The effect of endostatin evaluated in an experimental animal model of collagen-induced arthritisD Kurosaka, K Yoshida, J Yasuda, et al.
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|July 25, 2000
Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and humanH Yatsuki, H Watanabe, M Hattori, et al.
Clinical Genetics|December 5, 2013
A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patientK Higashimoto, K Jozaki, T Kosho, et al.
Epidemiology and Infection|October 17, 2015
Risk of haemolytic uraemic syndrome caused by shiga-toxin-producing Escherichia coli infection in adult women in JapanJ Fujii, T Mizoue, T Kita, et al.
Acta Paediatrica Japonica : Overseas Edition|September 24, 1998
An evaluation of infants' growth in the Kingdom of NepalS Hosono, M Okazaki, S Kagimoto, et al.
Clinical Genetics|August 30, 2014
Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndromeY Ohtsuka, K Higashimoto, K Sasaki, et al.
Human Genetics|September 16, 1998
Molecular and clinical study of 183 patients with conotruncal anomaly face syndromeR Matsuoka, M Kimura, P J Scambler, et al.
Journal of Korean Medical Science|April 18, 2001
Clinical impacts of tumor cell contamination of hematopoietic stem cell products in metastatic breast cancer patients undergoing autologous peripheral blood stem cell transplantation: multicenter trialM J Ahn, Y H Noh, Y S Lee, et al.
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