Cai SP - Search Results

1

Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype.

Waye JS, Chui DH, Eng B, Cai SP, Coleman MB, Adams JG 3rd, Steinberg MH. Waye JS, et al. Among authors: cai sp. Am J Hematol. 1991 Oct;38(2):108-12. doi: 10.1002/ajh.2830380207. Am J Hematol. 1991. PMID: 1719807

2

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

Waye JS, Cai SP, Eng B, Chui DH, Francombe WH. Waye JS, et al. Among authors: cai sp. Am J Hematol. 1992 Dec;41(4):289-91. doi: 10.1002/ajh.2830410413. Am J Hematol. 1992. PMID: 1283810

3

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

Cai SP, Eng B, Francombe WH, Olivieri NF, Kendall AG, Waye JS, Chui DH. Cai SP, et al. Blood. 1992 Mar 1;79(5):1342-6. Blood. 1992. PMID: 1536956 Free article.

4

A new frameshift beta zero-thalassemia mutation (codons 27-28 +C) found in a Chinese family.

Cai SP, Chui DH, Ng J, Poon AO, Freedman MH, Olivieri NF. Cai SP, et al. Am J Hematol. 1991 May;37(1):6-8. doi: 10.1002/ajh.2830370103. Am J Hematol. 1991. PMID: 1850955

5

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

Cai SP, Eng B, Kan YW, Chui DH. Cai SP, et al. Hum Genet. 1991 Oct;87(6):728-30. doi: 10.1007/BF00201734. Hum Genet. 1991. PMID: 1937477

6

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

Waye JS, Cai SP, Eng B, Clark C, Adams JG 3rd, Chui DH, Steinberg MH. Waye JS, et al. Among authors: cai sp. Blood. 1991 Mar 1;77(5):1100-3. Blood. 1991. PMID: 1995096 Free article.

7

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

Tang W, Cai SP, Eng B, Poon MC, Waye JS, Illum N, Chui DH. Tang W, et al. Among authors: cai sp. Blood. 1993 Mar 15;81(6):1636-40. Blood. 1993. PMID: 7680924 Free article.

8

Carrier detection and prenatal diagnosis of hemoglobinopathies in Ontario.

Waye JS, Eng B, Cai SP, Patterson M, Smith J, Tang W, Chui DH. Waye JS, et al. Among authors: cai sp. Clin Invest Med. 1993 Oct;16(5):358-71. Clin Invest Med. 1993. PMID: 8261689 Review.

9

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

Cai SP, Zhang JZ, Doherty M, Kan YW. Cai SP, et al. Am J Hum Genet. 1989 Jul;45(1):112-4. Am J Hum Genet. 1989. PMID: 2741940 Free PMC article.

10

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

Ballas SK, Cai SP, Gabuzda T, Chehab FF. Ballas SK, et al. Among authors: cai sp. Am J Med Genet. 1997 Mar 17;69(2):196-9. Am J Med Genet. 1997. PMID: 9056561 Review.

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