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Results:
1-21
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Results: 21
Authors:
Lorey, F
Cunningham, G
Vichinsky, EP
Lubin, BH
Witkowska, HE
Matsunaga, A
Azimi, M
Sherwin, J
Eastman, J
Farina, F
Waye, JS
Chui, DHK
Citation: F. Lorey et al., Universal newborn screening for Hb H disease in California, GENET TEST, 5(2), 2001, pp. 93-100
Authors:
Chui, DHK
Dover, GJ
Citation: Dhk. Chui et Gj. Dover, Sickle cell disease: no longer a single gene disorder, CURR OP PED, 13(1), 2001, pp. 22-27
Authors:
Horsley, SW
Daniels, RJ
Anguita, E
Raynham, HA
Peden, JF
Villegas, A
Vickers, MA
Green, S
Waye, JS
Chui, DHK
Ayyub, H
MacCarthy, AB
Buckle, VJ
Gibbons, RJ
Kearney, L
Higgs, DR
Citation: Sw. Horsley et al., Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects, EUR J HUM G, 9(3), 2001, pp. 217-225
Authors:
Hardison, RC
Chui, DHK
Riemer, C
Giardine, B
Lehvaslaiho, H
Wajcman, H
Miller, W
Citation: Rc. Hardison et al., Databases of human hemoglobin variants and other resources at the globin gene server, HEMOGLOBIN, 25(2), 2001, pp. 183-193
Novel beta-thalassemia mutation in a beta-thalassemia intermedia patient [poly A (AATAAA -> GATAAA)]
Authors:
Waye, JS
Eng, B
Patterson, M
Reis, MD
Macdonald, D
Chui, DHK
Citation: Js. Waye et al., Novel beta-thalassemia mutation in a beta-thalassemia intermedia patient [poly A (AATAAA -> GATAAA)], HEMOGLOBIN, 25(1), 2001, pp. 103-105
Authors:
Waye, JS
Eng, B
Patterson, M
Walker, L
Carcao, MD
Olivieri, NF
Chui, DHK
Citation: Js. Waye et al., Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases, AM J HEMAT, 68(1), 2001, pp. 11-15
Authors:
Lau, ET
Kwok, YK
Chui, DHK
Wong, HS
Hong, YLT
Tang, MHY
Citation: Et. Lau et al., Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures, PRENAT DIAG, 21(7), 2001, pp. 529-539
Authors:
Waye, JS
Chui, DHK
Citation: Js. Waye et Dhk. Chui, The alpha-globin gene cluster: genetics and disorders, CLIN INV M, 24(2), 2001, pp. 103-109
Authors:
Leung, KFS
Au, WY
Chan, AYY
Chan, LC
Waye, JS
Chui, DHK
Ma, SK
Citation: Kfs. Leung et al., Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family, CLIN LAB H, 23(1), 2001, pp. 53-55
Authors:
Chan, LC
Ma, SK
Chan, AYY
Ha, SY
Waye, JS
Lau, YL
Chui, DHK
Citation: Lc. Chan et al., Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?, J CLIN PATH, 54(4), 2001, pp. 317-320
Authors:
Lorey, F
Charoenkwan, P
Witkowska, HE
Lafferty, J
Patterson, M
Eng, B
Waye, JS
Finklestein, JZ
Chui, DHK
Citation: F. Lorey et al., Hb H hydrops foetalis syndrome: a case report and review of literature, BR J HAEM, 115(1), 2001, pp. 72-78
Authors:
Lafferty, JD
Crowther, MA
Waye, JS
Chui, DHK
Citation: Jd. Lafferty et al., A reliable screening test to identify adult carriers of the (--(SEA)) alpha(0)-thalassemia deletion - Detection of embryonic zeta-globin chains by enzyme-linked immunosorbent assay, AM J CLIN P, 114(6), 2000, pp. 927-931
Authors:
Ye, TZ
Gordon, CT
Lai, YH
Fujiwara, Y
Peters, LL
Perkins, AC
Chui, DHK
Citation: Tz. Ye et al., Ermap, a gene coding for a novel erythroid specific adhesion/receptor membrane protein, GENE, 242(1-2), 2000, pp. 337-345
Authors:
Waye, JS
Walker, L
Chui, DHK
Lafferty, J
Kirby, M
Citation: Js. Waye et al., Homozygous Hb Sallanches [alpha 104(G11)Cys -> Tyr] in a Pakistani child with Hb H disease, HEMOGLOBIN, 24(4), 2000, pp. 355-357
Authors:
Waye, JS
Eng, B
Chui, DHK
Powers, PJ
Lafferty, JD
Citation: Js. Waye et al., Second report of Hb Toulon [alpha 77(EF6)Pro -> His] in a Canadian family of Italian descent, HEMOGLOBIN, 24(4), 2000, pp. 359-360
Authors:
Ma, SK
Chow, EYD
Chan, AYY
Kung, NNS
Waye, JS
Chan, LC
Chui, DHK
Citation: Sk. Ma et al., beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay(beta codon 19 AAC -> AGC; Asn -> Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation, AM J HEMAT, 64(3), 2000, pp. 206-209
Authors:
Eng, B
Patterson, M
Borys, S
Chui, DHK
Waye, JS
Citation: B. Eng et al., PCR-based diagnosis of the Filipino (__(FIL)) and Thai (__(THAI)) alpha-thalassemia-1 deletions, AM J HEMAT, 63(1), 2000, pp. 54-56
Authors:
Ma, SK
Chan, AYY
Chan, LC
Chui, DHK
Waye, JS
Citation: Sk. Ma et al., Compound heterozygosity for triplicated alpha-globin gene and (- -(SEA)) alpha-globin gene deletion: Implication for thalassaemia screening, BR J HAEM, 110(2), 2000, pp. 498-499
Authors:
Carcao, MD
Chang, L
Poon, A
Olivieri, NF
Waye, JS
Eng, B
Patterson, M
Chui, DHK
Citation: Md. Carcao et al., Compound heterozygosity for Hb S and Hb G-Copenhagen, HEMOGLOBIN, 23(4), 1999, pp. 379-381
Authors:
Waye, JS
Borys, S
Eng, B
Patterson, M
Chui, DHK
El-Din, OMKB
Aref, MK
Afify, Z
Citation: Js. Waye et al., Spectrum of beta-thalassemia mutations in Egypt, HEMOGLOBIN, 23(3), 1999, pp. 255-261
Authors:
Luo, HY
Liang, XL
Frye, C
Wonio, M
Hankins, GDV
Chui, DHK
Alter, BP
Citation: Hy. Luo et al., Embryonic hemoglobins are expressed in definitive cells, BLOOD, 94(1), 1999, pp. 359-361
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