Can Liao

Ontology type: schema:Person     

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Publications in SciGraph latest 50 shown

  • 2017-12 Chromosome microarray analysis in the investigation of children with congenital heart disease in BMC PEDIATRICS
  • 2017-11 Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes in ARCHIVES OF GYNECOLOGY AND OBSTETRICS
  • 2016-12 Application of high resolution SNP arrays in patients with congenital oral clefts in south China in JOURNAL OF GENETICS
  • 2015-06 Implementation of Newborn Screening for Hemoglobin H Disease in Mainland China in INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION
  • 2014-01 The prevalence of non-detectable chromosomal abnormalities by QF-PCR in amniocentesis for certain referral indications: experience at a mainland Chinese hospital in ARCHIVES OF GYNECOLOGY AND OBSTETRICS
  • 2011-12 Ring chromosome 13 syndrome characterized by high resolution array based comparative genomic hybridization in patient with 47, XYY syndrome: a case report in JOURNAL OF MEDICAL CASE REPORTS
  • 2011-01 Mild hemoglobin H-constant spring disease with β-thalassemia—a case report in ANNALS OF HEMATOLOGY
  • 2010-03 A novel β-globin gene deletion (codons 89–93) in a Chinese family in ANNALS OF HEMATOLOGY
  • 2009-11 Diversity in clinical presentation of hemoglobin H disease induced by the SEA deletion and the hemoglobin Quong Sze in ANNALS OF HEMATOLOGY
  • 2009-11 A novel mutation of −50 (G→A) in the direct repeat element of the β-globin gene identified in a patient with severe β-thalassemia in ANNALS OF HEMATOLOGY
  • 2009-08 A novel β-thalassemic allele due to a thirteen nucleotide deletion: codons 54–58 (-T ATG GGC AAC CCT) in ANNALS OF HEMATOLOGY
  • 2009-07 The 4-bp deletion (-AAAC) in the 5′ untranslated region of the β-globin gene: a simple polymorphism? in ANNALS OF HEMATOLOGY
  • 2008-09 First detection of the codons 41–43 (−CTTTG,+A) β-thalassemia mutation in a Chinese patient in ANNALS OF HEMATOLOGY
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