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Can Liao

Showing results (21-30 of 300) with videos related to

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Annals of Hematology|April 4, 2008
First detection of the codons 41-43 (-CTTTG,+A) beta-thalassemia mutation in a Chinese patientCan Liao, Dong-Zhi Li, Jian Li
Prenatal Diagnosis|March 19, 2009
Prenatal diagnosis of hemoglobin Bart's disease caused by co-inheritance of two different alpha 0-thalassemia defects in ChinaDong-Zhi Li, Jian Li, Can Liao
Annals of Hematology|January 7, 2009
A novel beta-thalassemic allele due to a thirteen nucleotide deletion: codons 54-58 (-T ATG GGC AAC CCT)Dong-Zhi Li, Can Liao, Jian Li
Prenatal Diagnosis|July 23, 2008
Fetal anemia and hydrops associated with homozygosity for hemoglobin Quong SzeCan Liao, Jian Li, Dong-Zhi Li
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 15, 2010
Two cases of non-haematological cause of fetal hydrops in at-risk pregnancies for homozygous α0-thalassemiaJia-Xue Wei, Can Liao, Dong-Zhi Li
Prenatal Diagnosis|February 8, 2006
Homozygous alpha-thalassemia associated with micropenis in a fetusDong-Zhi Li, Can Liao, Qiu-Ming Li
Hemoglobin|June 27, 2006
The codon 37 (TGG-->TAG) beta(0)-thalassemia mutation found in a Chinese familyDongzhi Li, Can Liao, Jian Li, et al.
Haematologica|December 7, 2005
First detection of the splice donor site IVS-I-2 (T-->B) beta-thalassemia mutation in a Chinese patientCan Liao, Jian Li, Yining Huang, et al.
Hemoglobin|November 17, 2010
High-resolution melting analysis of the three common nondeletional α-thalassemia mutations in the Chinese population: Hbs Constant Spring, Quong Sze and WestmeadRu Li, Can Liao, Dongzhi Li, et al.
Prenatal Diagnosis|February 14, 2006
Amniocentesis for karyotyping prior to induction of abortion at second trimesterDongzhi Li, Can Liao, Cuixing Yi, et al.
Pageof 30

Showing results (21-30 of 300) with videos related to

Sort By:
Pageof 30
Annals of Hematology|April 4, 2008
First detection of the codons 41-43 (-CTTTG,+A) beta-thalassemia mutation in a Chinese patientCan Liao, Dong-Zhi Li, Jian Li
Prenatal Diagnosis|March 19, 2009
Prenatal diagnosis of hemoglobin Bart's disease caused by co-inheritance of two different alpha 0-thalassemia defects in ChinaDong-Zhi Li, Jian Li, Can Liao
Annals of Hematology|January 7, 2009
A novel beta-thalassemic allele due to a thirteen nucleotide deletion: codons 54-58 (-T ATG GGC AAC CCT)Dong-Zhi Li, Can Liao, Jian Li
Prenatal Diagnosis|July 23, 2008
Fetal anemia and hydrops associated with homozygosity for hemoglobin Quong SzeCan Liao, Jian Li, Dong-Zhi Li
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|October 15, 2010
Two cases of non-haematological cause of fetal hydrops in at-risk pregnancies for homozygous α0-thalassemiaJia-Xue Wei, Can Liao, Dong-Zhi Li
Prenatal Diagnosis|February 8, 2006
Homozygous alpha-thalassemia associated with micropenis in a fetusDong-Zhi Li, Can Liao, Qiu-Ming Li
Hemoglobin|June 27, 2006
The codon 37 (TGG-->TAG) beta(0)-thalassemia mutation found in a Chinese familyDongzhi Li, Can Liao, Jian Li, et al.
Haematologica|December 7, 2005
First detection of the splice donor site IVS-I-2 (T-->B) beta-thalassemia mutation in a Chinese patientCan Liao, Jian Li, Yining Huang, et al.
Hemoglobin|November 17, 2010
High-resolution melting analysis of the three common nondeletional α-thalassemia mutations in the Chinese population: Hbs Constant Spring, Quong Sze and WestmeadRu Li, Can Liao, Dongzhi Li, et al.
Prenatal Diagnosis|February 14, 2006
Amniocentesis for karyotyping prior to induction of abortion at second trimesterDongzhi Li, Can Liao, Cuixing Yi, et al.
Pageof 30