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Genetics and Molecular Biology|July 8, 2011
RUNX2 mutations in Taiwanese patients with cleidocranial dysplasiaWei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, et al.
Fertility and Sterility|October 24, 2007
Kabuki syndrome in a girl with mosaic 45,X/47,XXX and aortic coarctationChih-Ping Chen, Shuan-Pei Lin, Fuu-Jen Tsai, et al.
Fertility and Sterility|February 29, 2008
Characterization of a de novo unbalanced Y;autosome translocation in a 45,X mentally retarded male and literature reviewChih-Ping Chen, Shuan-Pei Lin, Fuu-Jen Tsai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 20, 2008
Genetic analysis of mucopolysaccharidosis type VI in Taiwanese patientsWei-De Lin, Shuan-Pei Lin, Chung-Hsing Wang, et al.
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 28, 2011
Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findingsChih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, et al.
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