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Genetic Counseling (Geneva, Switzerland)|May 23, 2007
Prenatal diagnosis and genetic counseling of mucopolysaccharidosis type II (Hunter syndrome)C P Chen, S P Lin, C Y Tzen, et al.Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactylyC-P Chen, S-P Lin, M-R Chen, et al.Tissue Engineering. Part A|August 22, 2025
Oxygenation and Temperature Conditioning Alter the Vascular Morphology of Microvascular ConstructsSamuel Nightheart, Adam Rauff, Ethan Dinh, et al.Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|September 12, 2001
Mutation analysis of type II Gaucher disease in five Taiwanese children: identification of two novel mutationsF J Tsai, C C Lee, M C Wu, et al.Advanced Healthcare Materials|February 22, 2023
Engineering of an Osteoinductive and Growth Factor-Free Injectable Bone-Like Microgel for Bone RegenerationRamesh Subbiah, Edith Y Lin, Avathamsa Athirasala, et al.Genetic Counseling (Geneva, Switzerland)|February 26, 2013
De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delayC-P Chen, S-P Lin, Y-L Huang, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 1, 1997
Clinical and perinatal sonographic features of congenital adrenal cystic neuroblastoma: a case report with review of the literatureC P Chen, S H Chen, C Y Chuang, et al.Proceedings of the National Academy of Sciences of the United States of America|November 9, 2004
Estrogen prevents bone loss through transforming growth factor beta signaling in T cellsYuhao Gao, Wei-Ping Qian, Kimberly Dark, et al.Investigative Ophthalmology & Visual Science|October 29, 2000
Growth and differentiation of human lens epithelial cells in vitro on matrixE A Blakely, K A Bjornstad, P Y Chang, et al.Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000
Molecular diagnosis of Apert syndrome in Chinese patientsF J Tsai, C H Tsai, C T Peng, et al.Pageof 25