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Can Liao

Showing results (171-180 of 301) with videos related to

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Prenatal Diagnosis|October 1, 2020
Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21Wenwen Zhang, Tingying Lei, Fang Fu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 4, 2006
[HLA-B gene polymorphism detected by high-resolution sequence-based typing in Guangdong Han populations]Yan Li, Xue-wei Tang, Jie-ying Wu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2010
[Application of array-based comparative genomic hybridization in precise diagnosis of unbalanced chromosome aberration]Fang Fu, Can Liao, Min Pan, et al.
Prenatal Diagnosis|April 9, 2020
Nonimmune hydrops fetalis: Genetic analysis and clinical outcomeQiong Deng, Fang Fu, Qiuxia Yu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 9, 2012
[Prenatal diagnosis of fetal urinary abnormalities and microdeletion on chromosome 1q21.1]Fang Fu, Yong-hua Huang, Can Liao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 7, 2016
[Application of chromosome microarray analysis for patients with skeletal anomalies and a normal karyotype]Qiaoli Guo, Fang Fu, Ru Li, et al.
Prenatal Diagnosis|March 28, 2013
Discordant results between fetal karyotyping and non-invasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescueMin Pan, Fa Tao Li, Yan Li, et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi|September 10, 2003
[Analysis of HLA matching probability in Guangzhou Cord Blood Bank]Yan Li, Can Liao, Xue-Wei Tang, et al.
Clinical Chemistry and Laboratory Medicine|October 26, 2011
Screening for mutations in the α-globin genes leading to abnormal hemoglobin variants with high resolution melting analysisYing-Na Liu, Ru Li, Jian-Ying Zhou, et al.
BMC Medical Genetics|March 1, 2020
Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern ChinaFan Jiang, Liandong Zuo, Dongzhi Li, et al.
Pageof 31

Showing results (171-180 of 301) with videos related to

Sort By:
Pageof 31
Prenatal Diagnosis|October 1, 2020
Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21Wenwen Zhang, Tingying Lei, Fang Fu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 4, 2006
[HLA-B gene polymorphism detected by high-resolution sequence-based typing in Guangdong Han populations]Yan Li, Xue-wei Tang, Jie-ying Wu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2010
[Application of array-based comparative genomic hybridization in precise diagnosis of unbalanced chromosome aberration]Fang Fu, Can Liao, Min Pan, et al.
Prenatal Diagnosis|April 9, 2020
Nonimmune hydrops fetalis: Genetic analysis and clinical outcomeQiong Deng, Fang Fu, Qiuxia Yu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 9, 2012
[Prenatal diagnosis of fetal urinary abnormalities and microdeletion on chromosome 1q21.1]Fang Fu, Yong-hua Huang, Can Liao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 7, 2016
[Application of chromosome microarray analysis for patients with skeletal anomalies and a normal karyotype]Qiaoli Guo, Fang Fu, Ru Li, et al.
Prenatal Diagnosis|March 28, 2013
Discordant results between fetal karyotyping and non-invasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescueMin Pan, Fa Tao Li, Yan Li, et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi|September 10, 2003
[Analysis of HLA matching probability in Guangzhou Cord Blood Bank]Yan Li, Can Liao, Xue-Wei Tang, et al.
Clinical Chemistry and Laboratory Medicine|October 26, 2011
Screening for mutations in the α-globin genes leading to abnormal hemoglobin variants with high resolution melting analysisYing-Na Liu, Ru Li, Jian-Ying Zhou, et al.
BMC Medical Genetics|March 1, 2020
Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern ChinaFan Jiang, Liandong Zuo, Dongzhi Li, et al.
Pageof 31