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    1. Lorey, F; Cunningham, G; Vichinsky, EP; Lubin, BH; Witkowska, HE; Matsunaga, A; Azimi, M; Sherwin, J; Eastman, J; Farina, F; Waye, JS; Chui, DHK
      Universal newborn screening for Hb H disease in California

      GENETIC TESTING
    2. Chui, DHK; Dover, GJ
      Sickle cell disease: no longer a single gene disorder

      CURRENT OPINION IN PEDIATRICS
    3. 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
      Monosomy for the most telomeric, gene-rich region of the short arm of human chromosome 16 causes minimal phenotypic effects

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Hardison, RC; Chui, DHK; Riemer, C; Giardine, B; Lehvaslaiho, H; Wajcman, H; Miller, W
      Databases of human hemoglobin variants and other resources at the globin gene server

      HEMOGLOBIN
    5. Waye, JS; Eng, B; Patterson, M; Reis, MD; Macdonald, D; Chui, DHK
      Novel beta-thalassemia mutation in a beta-thalassemia intermedia patient [poly A (AATAAA -> GATAAA)]

      HEMOGLOBIN
    6. Waye, JS; Eng, B; Patterson, M; Walker, L; Carcao, MD; Olivieri, NF; Chui, DHK
      Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases

      AMERICAN JOURNAL OF HEMATOLOGY
    7. Lau, ET; Kwok, YK; Chui, DHK; Wong, HS; Hong, YLT; Tang, MHY
      Embryonic and fetal globins are expressed in adult erythroid progenitor cells and in erythroid cell cultures

      PRENATAL DIAGNOSIS
    8. Waye, JS; Chui, DHK
      The alpha-globin gene cluster: genetics and disorders

      CLINICAL AND INVESTIGATIVE MEDICINE-MEDECINE CLINIQUE ET EXPERIMENTALE
    9. Leung, KFS; Au, WY; Chan, AYY; Chan, LC; Waye, JS; Chui, DHK; Ma, SK
      Haemoglobin Q-Thailand and hereditary spherocytosis in a Chinese family

      CLINICAL AND LABORATORY HAEMATOLOGY
    10. Chan, LC; Ma, SK; Chan, AYY; Ha, SY; Waye, JS; Lau, YL; Chui, DHK
      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?

      JOURNAL OF CLINICAL PATHOLOGY
    11. Lorey, F; Charoenkwan, P; Witkowska, HE; Lafferty, J; Patterson, M; Eng, B; Waye, JS; Finklestein, JZ; Chui, DHK
      Hb H hydrops foetalis syndrome: a case report and review of literature

      BRITISH JOURNAL OF HAEMATOLOGY
    12. Ye, TZ; Gordon, CT; Lai, YH; Fujiwara, Y; Peters, LL; Perkins, AC; Chui, DHK
      Ermap, a gene coding for a novel erythroid specific adhesion/receptor membrane protein

      GENE
    13. Waye, JS; Walker, L; Chui, DHK; Lafferty, J; Kirby, M
      Homozygous Hb Sallanches [alpha 104(G11)Cys -> Tyr] in a Pakistani child with Hb H disease

      HEMOGLOBIN
    14. Waye, JS; Eng, B; Chui, DHK; Powers, PJ; Lafferty, JD
      Second report of Hb Toulon [alpha 77(EF6)Pro -> His] in a Canadian family of Italian descent

      HEMOGLOBIN
    15. Ma, SK; Chow, EYD; Chan, AYY; Kung, NNS; Waye, JS; Chan, LC; Chui, DHK
      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

      AMERICAN JOURNAL OF HEMATOLOGY
    16. Eng, B; Patterson, M; Borys, S; Chui, DHK; Waye, JS
      PCR-based diagnosis of the Filipino (__(FIL)) and Thai (__(THAI)) alpha-thalassemia-1 deletions

      AMERICAN JOURNAL OF HEMATOLOGY
    17. Ma, SK; Chan, AYY; Chan, LC; Chui, DHK; Waye, JS
      Compound heterozygosity for triplicated alpha-globin gene and (- -(SEA)) alpha-globin gene deletion: Implication for thalassaemia screening

      BRITISH JOURNAL OF HAEMATOLOGY
    18. Lafferty, JD; Crowther, MA; Waye, JS; Chui, DHK
      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

      AJCP. American journal of clinical pathology
    19. Carcao, MD; Chang, L; Poon, A; Olivieri, NF; Waye, JS; Eng, B; Patterson, M; Chui, DHK
      Compound heterozygosity for Hb S and Hb G-Copenhagen

      HEMOGLOBIN
    20. Waye, JS; Borys, S; Eng, B; Patterson, M; Chui, DHK; El-Din, OMKB; Aref, MK; Afify, Z
      Spectrum of beta-thalassemia mutations in Egypt

      HEMOGLOBIN
    21. Luo, HY; Liang, XL; Frye, C; Wonio, M; Hankins, GDV; Chui, DHK; Alter, BP
      Embryonic hemoglobins are expressed in definitive cells

      BLOOD
    22. HARDISON R; RIEMER C; CHUI DHK; HUISMAN THJ; MILLER W
      ELECTRONIC ACCESS TO SEQUENCE ALIGNMENTS, EXPERIMENTAL RESULTS, AND HUMAN MUTATIONS AS AN AID TO STUDYING GLOBIN GENE-REGULATION

      Genomics
    23. HARDISON RC; CHUI DHK; RIEMER CR; MILLER W; CARVER MFH; MOLCHANOVA TP; EFREMOV GD; HUISMAN THJ
      ACCESS TO A SYLLABUS OF HUMAN HEMOGLOBIN-VARIANTS (1996) VIA THE WORLD-WIDE-WEB

      Hemoglobin
    24. WAYE JS; ENG B; PATTERSON M; CHUI DHK; FERNANDES BJ
      NOVEL BETA-THALASSEMIA MUTATION IN PATIENTS OF JEWISH DESCENT - [BETA-30(B12)ARG-]GLY OR IVS-I(-2)(A-]G)]

      Hemoglobin
    25. KRISHNAMURTI L; CHUI DHK; DALLAIRE M; LEROY B; WAYE JS; PERENTESIS JP
      COINHERITANCE OF ALPHA-THALASSEMIA-1 AND HEMOGLOBIN E BETA(0)-THALASSEMIA - PRACTICAL IMPLICATIONS FOR NEONATAL SCREENING AND GENETIC-COUNSELING/

      The Journal of pediatrics
    26. CHUI DHK; HARDISON R; RIEMER C; MILLER W; CARVER MFH; MOLCHANOVA TP; EFREMOV GD; HUISMAN THJ
      AN ELECTRONIC DATABASE OF HUMAN HEMOGLOBIN-VARIANTS ON THE WORLD-WIDE-WEB - COMMENTARY

      Blood
    27. CHUI DHK; WAYE JS
      HYDROPS-FETALIS CAUSED BY ALPHA-THALASSEMIA - AN EMERGING HEALTH-CAREPROBLEM

      Blood
    28. TANG WZ; LAI YH; HAN XD; WONG PMC; PETERS LL; CHUI DHK
      MURINE HN1 ON CHROMOSOME-11 IS EXPRESSED IN HEMATOPOIETIC AND BRAIN-TISSUES

      Mammalian genome
    29. WAYE JS; ENG B; PATTERSON M; CHUI DHK; NISBETBROWN E; OLIVIERI NF
      NOVEL MUTATION OF THE ALPHA-2-GLOBIN GENE INITIATION CODON (ATG-]A-G)IN A VIETNAMESE GIRL WITH HB-H DISEASE

      Hemoglobin
    30. WAYE JS; ENG B; PATTERSON M; CHUI DHK; FERNANDES BJ
      NOVEL BETA-DEGREES-THALASSEMIA MUTATION IN A CANADIAN WOMAN OF BRITISH DESCENT (CODONS-72 73,-AGTGA,+T)/

      Hemoglobin
    31. WAYE JS; ENG B; PATTERSON M; BARR RD; CHUI DHK
      DE-NOVO MUTATION OF THE BETA-GLOBIN GENE INITIATION CODON (ATG-]AAG) IN A NORTHERN EUROPEAN BOY

      American journal of hematology
    32. LAU YL; CHAN LC; CHAN YYA; HA SY; YEUNG CY; WAYE JS; CHUI DHK
      PREVALENCE AND GENOTYPES OF ALPHA-THALASSEMIA AND BETA-THALASSEMIA CARRIERS IN HONG-KONG - IMPLICATIONS FOR POPULATION SCREENING

      The New England journal of medicine
    33. WAYE JS; CHUI DHK
      BETA-THALASSEMIA DUE TO A 17 BASEPAIR DELETION

      British Journal of Haematology
    34. HARDISON RC; RIEMER C; MILLER W; CHUI DHK; MOLCHANOVA TP; CARVER MFH; EFREMOV GD; BAYSAL E; HUISMAN THJ
      ELECTRONIC AND PRINTED SYLLABI DESCRIBING 1) HUMAN HEMOGLOBIN-VARIANTS AND 2) DETERMINANTS OF THALASSEMIA AND HPFH

      Blood
    35. BORYS S; PATTERSON M; ENG B; CHUI DHK; ELDIN OMKB; AREF MK; AFIFY ZAM; WAYE JS
      BROAD-SPECTRUM OF BETA-THALASSEMIA MUTATIONS IN ALEXANDRIA, EGYPT

      Blood
    36. WAYE JS; ENG B; PATTERSON M; CHUI DHK; OLIVIERI NF
      NOVEL MUTATION OF THE ALPHA-2-GLOBIN GENE INITIATION CODON (ATG-]A-G)IN A VIETNAMESE GIRL WITH HB-H DISEASE

      Blood
    37. CHUI DHK; TANG W; LAI Y; ORKIN SH; LIEW CC
      EXPRESSED SEQUENCE TAG (EST) ANALYSIS OF MURINE YOLK-SAC DERIVED EMBRYONIC ERYTHROID-CELLS

      Blood
    38. WAYE JS; ENG B; FRANCOMBE WH; CHUI DHK
      NOVEL-17 BASEPAIR DELETION IN EXON-3 OF THE BETA-GLOBIN GENE

      Human mutation
    39. WAYE JS; ENG B; PATTERSON M; WASI P; CHUI DHK; FRANCOMBE WH; SHER GD; OLIVIERI NF
      SEVERITY OF BETA-THALASSEMIA DUE TO GENOTYPES INVOLVING THE IVS-I-6 (T-]C) MUTATION

      American journal of hematology
    40. CHAN LC; SO JCC; CHUI DHK
      COMPARISON OF HEMOGLOBIN-H INCLUSION-BODIES WITH EMBRYONIC ZETA-GLOBIN IN SCREENING FOR ALPHA-THALASSEMIA

      Journal of Clinical Pathology
    41. LUO HY; DEISSEROTH AB; CHUI DHK
      HUMAN EMBRYONIC ZETA-GLOBIN GENE-EXPRESSION IN MOUSE-HUMAN HYBRID ERYTHROID CELL-LINES

      Blood
    42. WAYE JS; CHUI DHK; HIGGS DR; HETHERINGTON R; OLIVIERI NF
      DE-NOVO DELETION OF THE ENTIRE ZETA-ALPHA GLOBIN GENE-CLUSTER IN A GIRL WITH HB-H DISEASE

      Blood
    43. CHUI DHK; TANG W; ORKIN SH; LIEW CC
      IDENTIFICATION OF GENES DURING MURINE EMBRYONIC ERYTHROPOIESIS

      Blood
    44. CHUI DHK; TANG WZ; ORKIN SH
      CDNA CLONING OF MURINE NRF2 GENE, CODING FOR A P45 NF-E2 RELATED TRANSCRIPTION FACTOR

      Biochemical and biophysical research communications
    45. HAIN RDW; CHITAYAT D; COOPER R; BANDLER E; ENG B; CHUI DHK; WAYE JS; FREEDMAN MH
      HB FM-FORT RIPLEY - CONFIRMATION OF AUTOSOMAL-DOMINANT INHERITANCE AND DIAGNOSIS BY PCR AND DIRECT NUCLEOTIDE SEQUENCING

      Human mutation
    46. HARADA F; IRELAND JH; HSIA YE; CHUI DHK
      ANTI-ZETA ANTIBODY SCREENING FOR ALPHA-THALASSEMIA USING DRIED FILTER-PAPER BLOOD

      Biochemical medicine and metabolic biology
    47. WAYE JS; ENG B; PATTERSON M; CHUI DHK; CHANG LS; COGIONIS B; POON AO; OLIVIERI NF
      HB E HB LEPORE(HOLLANDIA) IN A FAMILY FROM BANGLADESH

      American journal of hematology
    48. WAYE JS; PATTERSON M; ENG B; CHUI DHK; SHER GD; OLIVIERI NF
      DNA DIAGNOSIS OF HB-S AND HB-CARIBBEAN (ALPHA(2)BETA(91-LEU-]ARG)(2))IN A JAMAICAN FAMILY

      American journal of hematology
    49. WAYE JS; ENG B; HUNT JA; CHUI DHK
      FILIPINO BETA-THALASSEMIA DUE TO A LARGE DELETION - IDENTIFICATION OFTHE DELETION END-POINTS AND POLYMERASE CHAIN-REACTION (PCR)-BASED DIAGNOSIS

      Human genetics
    50. WAYE JS; ENG B; OLIVIERI NF; CHUI DHK
      IDENTIFICATION OF A NOVEL BETA(0)-THALASSEMIA MUTATION IN A GREEK FAMILY AND SUBSEQUENT PRENATAL-DIAGNOSIS

      Prenatal diagnosis
    51. WAYE JS; ENG B; PATTERSON M; CHUI DHK; OLIVIERI NF
      IDENTIFICATION OF A NOVEL TERMINATION CODON MUTATION (TAA-]TAT, TERM-]TYR) IN THE ALPHA-2 GLOBIN GENE OF A LAOTIAN GIRL WITH HEMOGLOBIN-H DISEASE

      Blood
    52. ENG B; CHUI DHK; SAUNDERSON J; OLIVIERI NF; WAYE JS
      IDENTIFICATION OF 2 NOVEL BETA-DEGREES-THALASSEMIA MUTATIONS IN A FILIPINO FAMILY - FRAMESHIFT CODON 67 (-TG) AND A BETA-DEGREES-GLOBIN GENE DELETION

      Human mutation
    53. IRELAND JH; LUO HY; CHUI DHK; CHU B; YUEN J; HSIA YE
      DETECTION OF THE (--(SEA)) DOUBLE ALPHA-GLOBIN GENE DETECTION BY A SIMPLE IMMUNOLOGICAL ASSAY FOR EMBRYONIC ZETA-GLOBIN CHAINS

      American journal of hematology
    54. WAYE JS; ENG B; CAI SP; PATTERSON M; SMITH J; TANG WZ; CHUI DHK
      CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF HEMOGLOBINOPATHIES IN ONTARIO

      Clinical and investigative medicine
    55. TANG WZ; LUO HY; ENG B; WAYE JS; CHUI DHK
      IMMUNOCYTOLOGICAL TEST TO DETECT ADULT CARRIERS OF (--SEA ) DELETIONAL ALPHA-THALASSEMIA/

      Lancet
    56. WAYE JS; ENG B; PATTERSON M; OLIVIERI NF; DOYLE JJ; CHUI DHK
      IDENTIFICATION OF A NOVEL TERMINATION CODON MUTATION (TAA-]TAT) IN THE ALPHA-2 GLOBIN GENE OF A GIRL WITH HEMOGLOBIN-H DISEASE

      Blood
    57. WAYE JS; ENG B; PATTERSON M; CHUI DHK
      PRENATAL-DIAGNOSIS OF HEMOGLOBINOPATHIES IN ONTARIO - A REVIEW OF 100CASES

      Blood
    58. WAYE JS; ENG B; PATTERSON M; CHUI DHK
      SPECTRUM OF BETA-THALASSEMIA MUTATIONS IN ONTARIO - 3 NOVEL FRAMESHIFT MUTATIONS IDENTIFIED BY NUCLEOTIDE SEQUENCING

      Blood
    59. TANG W; SANKAR U; ENG B; WAYE JS; CHUI DHK
      RAPID IMMUNOCYTOLOGICAL SCREENING FOR ADULT CARRIERS OF THE SOUTHEAST-ASIAN ALPHA-THALASSEMIA-1 DELETION (SEA)

      American journal of human genetics
    60. WAYE JS; OLIVIERI NF; SAUNDERSON J; CHUI DHK
      SPECTRUM OF BETA-THALASSEMIA MUTATIONS IN GREEK-CANADIANS - IDENTIFICATION OF A NOVEL CIRCLE-THALASSEMIA MUTATION, FRAMESHIFT CODONS 9 10(+T)/

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/08/20 alle ore 17:52:14