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Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|July 1, 1990
Isovaleric acidemia: report of one caseJ W Hou, T R WangJournal of the Formosan Medical Association = Taiwan Yi Zhi|May 1, 1995
Idiopathic juvenile osteoporosis: five-year case follow-upJ W Hou, T R WangJournal of the Formosan Medical Association = Taiwan Yi Zhi|June 1, 1996
Prader-Willi syndrome: clinical and molecular cytogenetic investigationsJ W Hou, T R WangClinical Genetics|September 1, 1995
Molecular cytogenetic studies of duplication 9q32-->q34.3 inserted into 9q13J W Hou, T R WangCritical Reviews in Microbiology|January 1, 1994
Pneumococcal infection and immunization in childrenC J Lee, T R WangZhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|May 1, 1995
Transient tyrosinemia presenting as lactic acidosis in a term baby: report of one caseJ W Hou, T R WangAmerican Journal of Human Genetics|March 7, 2001
Cloning of dimethylglycine dehydrogenase and a new human inborn error of metabolism, dimethylglycine dehydrogenase deficiencyB A Binzak, R A Wevers, S H Moolenaar, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 24, 2006
Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotypeM Chen, W-L Hwu, S-J Kuo, et al.Journal of Medical Genetics|December 10, 1997
Mucopolysaccharidosis type I: identification of novel mutations that cause Hurler/Scheie syndrome in Chinese familiesG J Lee-Chen, T R WangMolecular Genetics and Metabolism|August 7, 2009
Miglustat in patients with Niemann-Pick disease Type C (NP-C): a multicenter observational retrospective cohort studyM Pineda, J E Wraith, E Mengel, et al.Pageof 17