Waye JS - Search Results

1

Coinheritance of alpha-thalassemia-1 and hemoglobin E/beta zero-thalassemia: practical implications for neonatal screening and genetic counseling.

Krishnamurti L, Chui DH, Dallaire M, LeRoy B, Waye JS, Perentesis JP. Krishnamurti L, et al. Among authors: waye js. J Pediatr. 1998 May;132(5):863-5. doi: 10.1016/s0022-3476(98)70319-1. J Pediatr. 1998. PMID: 9602201

2

Prevalence and genotypes of alpha- and beta-thalassemia carriers in Hong Kong -- implications for population screening.

Lau YL, Chan LC, Chan YY, Ha SY, Yeung CY, Waye JS, Chui DH. Lau YL, et al. Among authors: waye js. N Engl J Med. 1997 May 1;336(18):1298-301. doi: 10.1056/NEJM199705013361805. N Engl J Med. 1997. PMID: 9113933 Free article.

3

A reliable screening test to identify adult carriers of the (--SEA) alpha zero-thalassemia deletion. Detection of embryonic zeta-globin chains by enzyme-linked immunosorbent assay.

Lafferty JD, Crowther MA, Waye JS, Chui DH. Lafferty JD, et al. Among authors: waye js. Am J Clin Pathol. 2000 Dec;114(6):927-31. doi: 10.1309/26G7-BQH4-93BV-UR0Q. Am J Clin Pathol. 2000. PMID: 11338482

4

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. Am J Hematol. 1991 Oct;38(2):108-12. doi: 10.1002/ajh.2830380207. Am J Hematol. 1991. PMID: 1719807

5

High hemoglobin A2 beta-thalassemia.

Steinberg MH, Coleman MB, Adams JG 3rd, Waye JS, Chui DH. Steinberg MH, et al. Among authors: waye js. J Lab Clin Med. 1991 Oct;118(4):382. J Lab Clin Med. 1991. PMID: 1940581 No abstract available.

6

Identification of two novel beta zero-thalassemia mutations in a Filipino family: frameshift codon 67 (-TG) and a beta-globin gene deletion.

Eng B, Chui DH, Saunderson J, Olivieri NF, Waye JS. Eng B, et al. Among authors: waye js. Hum Mutat. 1993;2(5):375-9. doi: 10.1002/humu.1380020509. Hum Mutat. 1993. PMID: 8257991

7

Hydrops fetalis caused by alpha-thalassemia: an emerging health care problem.

Chui DH, Waye JS. Chui DH, et al. Among authors: waye js. Blood. 1998 Apr 1;91(7):2213-22. Blood. 1998. PMID: 9516118 Free article. Review. No abstract available.

8

PCR-based diagnosis of the Filipino (--(FIL)) and Thai (--(THAI)) alpha-thalassemia-1 deletions.

Eng B, Patterson M, Borys S, Chui DH, Waye JS. Eng B, et al. Among authors: waye js. Am J Hematol. 2000 Jan;63(1):54-6. doi: 10.1002/(sici)1096-8652(200001)63:1<54::aid-ajh12>3.0.co;2-b. Am J Hematol. 2000. PMID: 10602170 Free article.

9

Detection of severe nondeletional alpha-thalassemia mutations using a single-tube multiplex ARMS assay.

Eng B, Patterson M, Walker L, Chui DH, Waye JS. Eng B, et al. Among authors: waye js. Genet Test. 2001 Winter;5(4):327-9. doi: 10.1089/109065701753617471. Genet Test. 2001. PMID: 11960579

10

Hb Evora [alpha 2-35, Ser-->Pro], a novel hemoglobin variant associated with an alpha-thalassemia phenotype.

Waye JS, Chui DH. Waye JS, et al. Haematologica. 2007 May;92(5):e68. doi: 10.3324/haematol.11572. Haematologica. 2007. PMID: 17562600 Free article. No abstract available.

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