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European Journal of Medical Genetics|March 30, 2010
Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delayChih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, et al.
Taiwanese Journal of Obstetrics & Gynecology|July 17, 2012
Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcomeChih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, et al.
Current Medicinal Chemistry|October 16, 2024
Development and Validation of a Cholesterol-related Gene Signature for Prognostic Assessment in Head and Neck Squamous Cell CarcinomaJiarong Zheng, Dalong Shu, Rongwei Xu, et al.
Kidney International|March 29, 2002
Tubular and cellular localization of the cardiac L-type calcium channel in rat kidneyPei-Lin Zhao, Xi-Tao Wang, Xue-Mei Zhang, et al.
Clinical and Translational Science|October 6, 2022
Comparative effectiveness and safety of extended anticoagulant therapy among Medicare beneficiaries with venous thromboembolismHaesuk Park, Hye-Rim Kang, Pei-Lin Huang, et al.
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