|1.||Li, Dong-Zhi: 5 articles (01/2014 - 09/2008)|
|2.||Liao, Can: 4 articles (09/2013 - 09/2008)|
|3.||Li, Jian: 3 articles (09/2013 - 09/2008)|
|4.||Zhou, Jian-Ying: 3 articles (09/2013 - 11/2009)|
|5.||Xie, Xing-Mei: 3 articles (09/2013 - 11/2009)|
|6.||Li, Ru: 2 articles (09/2013 - 01/2012)|
|7.||Tan, Mei: 1 article (10/2015)|
|8.||Lu, Sen: 1 article (10/2015)|
|9.||Jin, Da-Wei: 1 article (10/2015)|
|10.||Wu, Liu-Song: 1 article (10/2015)|
11/01/2009 - "Diversity in clinical presentation of hemoglobin H disease induced by the SEA deletion and the hemoglobin Quong Sze."
09/01/2007 - "Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method."
07/01/2003 - "Rapid detection of an a thalassemia variant (Hb Quong Sze)."
01/01/1998 - "For alpha-thalassemia 2, the rightward deletion is the most common, followed by the leftward deletion, and the nondeletional defects Hb Constant Spring and Hb Quong Sze. "
05/01/2007 - "Five mutations account for 98% of alpha-thalassemia [--SEA 46.7%; -alpha/4.2, 23.9%; -alpha/3.7, 21.7%; hemoglobin (Hb) Constant Spring, 6.5%; Hb Quong Sze, 1.1%]. "
05/01/2014 - "Of the 55 α-thalassemia carriers, five different deletions of α-thalassemia were identified, the three most common deletion types and proportions were 54.55% for the -α(3.7) deletion, 18.18% for --(SEA) deletion, and 9.08% for the -α(4.2) deletion, respectively; eight types of nondeletion defects were determined, containing one case of Hb Quong Sze and seven novel mutations of a-globin gene. "
01/01/2014 - "Hb Quong Sze [Hb QS, HBA2: c.377T > C (or HBA1)] is a common nondeletional thalassemia in southern China. "
01/01/2014 - "Screening and diagnosis of Hb Quong Sze [HBA2: c.377T > C (or HBA1)] in a prenatal control program for thalassemia."
09/01/2013 - "All couples were screened for α-thalassemia trait, and for couples in whom one partner was tested positive for α(0) -thalassemia, the other was subjected to screening for Hb Constant Spring and Hb Quong Sze mutations. "
01/01/2012 - "Hb Constant Spring (Hb CS, α142, TAA>CAA at α2) and Hb Quong Sze [Hb QS, α125, CTG>CCG (α2)] are the most common nondeletional α-thalassemias in the Chinese population. "
|1.||Hemoglobin Constant Spring
|2.||Glycosylated Hemoglobin A (Glycosylated Hemoglobin)