S. Cai

发表

Rapid prenatal diagnosis of beta thalassemia using DNA amplification and nonradioactive probes.

R. Saiki, Y. Kan, H. Erlich, 1989, Blood.

A short-term trial of butyrate to stimulate fetal-globin-gene expression in the beta-globin disorders.

D. Faller, H. Witkowska, N. Olivieri, 1993, The New England journal of medicine.

Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario.

W. Tang, D. Chui, B. Eng, 1993, Clinical and investigative medicine. Medecine clinique et experimentale.

A new frameshift β°‐thalassemia mutation (codons 27–28 +C) found in a Chinese family

M. Freedman, N. Olivieri, A. Poon, 1991 .

Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene.

N. Olivieri, D. Chui, B. Eng, 1992, Blood.

Identification of the multiple beta-thalassemia mutations by denaturing gradient gel electrophoresis.

S. Cai, Y. Kan, 1990, The Journal of clinical investigation.

Prenatal diagnosis of unusual hemoglobinopathies.

R. Lebo, M. Golbus, J. Chung, 1994, American journal of medical genetics.

Beta-thalassemia mutations in Indonesia and their linkage to beta haplotypes.

M. Lim, S. Cai, Y. Kan, 1989, American journal of human genetics.

A new TATA box mutation detected at prenatal diagnosis for beta-thalassemia.

S. Cai, J. Z. Zhang, Y. Kan, 1989, American journal of human genetics.

Reverse dot blot probes for the screening of β‐thalassernia mutationsin Asians and American blacks

J. Wall, Y. Kan, F. Chehab, 1994 .

Molecular basis of β thalassemia in South China

Y. Kan, F. Chehab, S. Cai, 2004, Human Genetics.

Molecular basis of asymptomatic beta-thalassemia major in an African American individual.

F. Chehab, S. Ballas, S. Cai, 1997, American journal of medical genetics.

Hb S/β°‐Thalassemia due to the ˜1.4‐kb deletion is associated with a relatively mild phenotype

M. Steinberg, D. Chui, B. Eng, 1991 .

High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region.

D. Chui, B. Eng, J. Waye, 1991, Blood.

Reverse dot blot probes for the screening of beta-thalassemia mutations in Asians and American blacks.

J. Wall, Y. Kan, F. Chehab, 1994, Human mutation.

Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily.

Jeffrey D. Wall, J. Wall, Y. Kan, 1993, Blood.

Prenatal Diagnosis of Thalassemia in South China a

Y. Kan, S. Cai, Jizeng Zhang, 1990, Annals of the New York Academy of Sciences.

Molecular basis of beta thalassemia in south China. Strategy for DNA analysis.

Y. Kan, F. Chehab, S. Cai, 1988, Human genetics.

Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemia.

M. Poon, D. Chui, B. Eng, 1993, Blood.

Identification of the Multiple ,B-Thalassemia Mutations by Denaturing Gradient Gel Electrophoresis

S. Cai, Y. Kan, 2013 .

A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to β-thalassemia

Y. Kan, D. Chui, B. Eng, 1991, Human Genetics.

The Use of Direct Gene Analysis to Define β‐Thalassemia a

Y. Kan, F. Chehab, S. Cai, 1990 .

A simple approach to prenatal diagnosis of beta-thalassemia in a geographic area where multiple mutations occur.

Y. Kan, S. Cai, J. Z. Zhang, 1988, Blood.

Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin kenya

D. Chui, B. Eng, J. Waye, 1992, American journal of hematology.

Hemoglobin constant spring defined by specific oligonucleotide hybridization and hemoglobin D Punjab (β121→Gln) in a Batak Indonesian family

Y. Kan, S. Cai, L. Lie-injo, 1988, American journal of hematology.

regions of the beta-globin gene (see comments) Two novel beta-thalassemia mutations in the 5' and 3' noncoding

N. Olivieri, D. Chui, B. Eng, 2011 .

A 31‐mutation assay for cystic fibrosis testing in the clinical molecular diagnostics laboratory

F. Chehab, S. Cai, Jeff Wall, 1995, Human mutation.

The use of direct gene analysis to define beta-thalassemia.

F. Chehab, S. Cai, A. Dozy, 1990, Annals of the New York Academy of Sciences.