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Journal 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 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 WangJournal of the Formosan Medical Association = Taiwan Yi Zhi|April 1, 1996
Double aneuploidy with Down's-Klinefelter's syndromeJ W Hou, T R WangJournal of the Formosan Medical Association = Taiwan Yi Zhi|November 1, 1994
Cytogenetic investigations in trisomy 21 with reciprocal 4/9 translocation: report of a caseJ W Hou, T R WangEuropean Journal of Pediatrics|March 21, 1998
Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in TaiwanJ W Hou, T R WangZhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|September 1, 1990
Restriction fragment length polymorphisms at the methylmalonyl CoA mutase locus in normal ChineseT R Wang, J W Hou, H M TsaiJournal of the Formosan Medical Association = Taiwan Yi Zhi|February 1, 1997
Microdeletion oe chromosomal region 7Q11.23 in Williams syndromeJ W Hou, J K Wang, T R WangJournal of the Formosan Medical Association = Taiwan Yi Zhi|August 12, 1999
Detection of KAL-1 gene deletion with fluorescence in situ hybridizationJ W Hou, W Y Tsai, T R WangZhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|July 1, 1990
Restriction fragment length polymorphisms at the ornithine transcarbamylase locus in normal ChineseT R Wang, J W Hou, H M TsaiPageof 16