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Molecular Genetics and Metabolism|October 6, 2005
DHPLC in clinical molecular diagnostic servicesKenjiro Kosaki, Toru Udaka, Torayuki Okuyama
Journal of Orthopaedic Science : Official Journal of the Japanese Orthopaedic Association|September 17, 2020
Impact of comorbidities on oncological outcomes of Japanese patients with high grade soft tissue sarcomasTakeshi Morii, Takashi Tajima, Toru Udaka, et al.
Endocrine Journal|September 9, 2006
Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutationTsutomu Ogata, Ikuma Fujiwara, Eishin Ogawa, et al.
Genetic Testing|January 27, 2007
Screening for CHARGE syndrome mutations in the CHD7 gene using denaturing high-performance liquid chromatographyMichihiko Aramaki, Toru Udaka, Chiharu Torii, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 7, 2006
Embryonic expression profile of chicken CHD7, the ortholog of the causative gene for CHARGE syndromeMichihiko Aramaki, Tokuhiro Kimura, Toru Udaka, et al.
Genetic Testing|June 10, 2005
Comprehensive screening of the thiopurine methyltransferase polymorphisms by denaturing high-performance liquid chromatographyToru Udaka, Chiharu Torii, Daisuke Takahashi, et al.
American Journal of Medical Genetics. Part A|March 6, 2007
An Alu retrotransposition-mediated deletion of CHD7 in a patient with CHARGE syndromeToru Udaka, Nobuhiko Okamoto, Michihiko Aramaki, et al.
Genetic Testing|October 24, 2007
Multiplex PCR/liquid chromatography assay for screening of subtelomeric rearrangementsToru Udaka, Issei Imoto, Yoshinori Aizu, et al.
Case Reports in Oncology|November 25, 2015
Langerhans Cell Histiocytosis of the Clavicle in an Adult: A Case Report and Review of the LiteratureToru Udaka, Michiro Susa, Kazutaka Kikuta, et al.
Congenital Anomalies|December 20, 2005
Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatographyToru Udaka, Hazuki Samejima, Rika Kosaki, et al.
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