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Results: 1-12 |
Results: 12
THE MOLECULAR-BASIS OF B-THALASSEMIA INTERMEDIA IN LEBANON
Authors: QATANANI MT TAHER A KOUSSA S DANA R OLD J ZAHED L
Citation: Mt. Qatanani et al., THE MOLECULAR-BASIS OF B-THALASSEMIA INTERMEDIA IN LEBANON, British Journal of Haematology, 102(1), 1998, pp. 48-48
AUDIT OF PRENATAL-DIAGNOSIS FOR HEMOGLOBIN DISORDERS IN THE UNITED-KINGDOM - THE FIRST 20 YEARS
Authors: MODELL B PETROU M LAYTON M VARNAVIDES L SLATER C WARD RHT RODECK C NICOLAIDES K GIBBONS S FITCHES A OLD J
Citation: B. Modell et al., AUDIT OF PRENATAL-DIAGNOSIS FOR HEMOGLOBIN DISORDERS IN THE UNITED-KINGDOM - THE FIRST 20 YEARS, BMJ. British medical journal, 315(7111), 1997, pp. 779-784
INCIDENCE OF ENDOCRINE COMPLICATIONS AND CLINICAL-DISEASE SEVERITY RELATED TO GENOTYPE ANALYSIS AND IRON OVERLOAD IN PATIENTS WITH BETA-THALASSEMIA
Authors: JENSEN CE TUCK SM OLD J MORRIS RW YARDUMIAN A DESANCTIS V HOFFBRAND AV WONKE B
Citation: Ce. Jensen et al., INCIDENCE OF ENDOCRINE COMPLICATIONS AND CLINICAL-DISEASE SEVERITY RELATED TO GENOTYPE ANALYSIS AND IRON OVERLOAD IN PATIENTS WITH BETA-THALASSEMIA, European journal of haematology, 59(2), 1997, pp. 76-81
ALPHA-THALASSEMIA AND SICKLE-CELL HEMOGLOBIN IN RELATION TO INFANT ANEMIA AND MALARIA
Authors: CHIMSUKU L BRABIN B VERHOEFF F BROADHEAD R OLD J RUSSELL W
Citation: L. Chimsuku et al., ALPHA-THALASSEMIA AND SICKLE-CELL HEMOGLOBIN IN RELATION TO INFANT ANEMIA AND MALARIA, The FASEB journal, 11(9), 1997, pp. 2337-2337
THE SPECTRUM OF BETA-THALASSEMIA MUTATIONS IN THE LEBANON
Authors: ZAHED L TALHOUK R SALEH M ABOUJAOUDEH R FISHER C OLD J
Citation: L. Zahed et al., THE SPECTRUM OF BETA-THALASSEMIA MUTATIONS IN THE LEBANON, Human heredity, 47(5), 1997, pp. 241-249
HEMOGLOBINOPATHIES
Authors: OLD J
Citation: J. Old, HEMOGLOBINOPATHIES, Prenatal diagnosis, 16(13), 1996, pp. 1181-1186
THE UNEXPECTED CO-INHERITANCE OF HOMOZYGOUS BETA-THALASSEMIA AND HBH DISEASE HIGHLIGHTS THE COMPLEXITIES OF HEMOGLOBINOPATHY SCREENING AND COUNSELING
Authors: MAY A POYSER H SHANKLEMAN J WEBB D KING L OLD J
Citation: A. May et al., THE UNEXPECTED CO-INHERITANCE OF HOMOZYGOUS BETA-THALASSEMIA AND HBH DISEASE HIGHLIGHTS THE COMPLEXITIES OF HEMOGLOBINOPATHY SCREENING AND COUNSELING, British Journal of Haematology, 93, 1996, pp. 338-338
OPTIMIZATION AND PROPERTIES OF A UHG FOR GENOTYPING OF HEMOGLOBIN-S AND HEMOGLOBIN-C
Authors: WOOD N STANDEN G OLD J BIDWELL J
Citation: N. Wood et al., OPTIMIZATION AND PROPERTIES OF A UHG FOR GENOTYPING OF HEMOGLOBIN-S AND HEMOGLOBIN-C, Human mutation, 5(2), 1995, pp. 166-172
MUTATIONAL BIAS PROVIDES A MODEL FOR THE EVOLUTION OF HUNTINGTONS-DISEASE AND PREDICTS A GENERAL INCREASE IN DISEASE PREVALENCE
Authors: RUBINSZTEIN DC AMOS W LEGGO J GOODBURN S RAMESAR RS OLD J BONTROP R MCMAHON R BARTON DE FERGUSONSMITH MA
Citation: Dc. Rubinsztein et al., MUTATIONAL BIAS PROVIDES A MODEL FOR THE EVOLUTION OF HUNTINGTONS-DISEASE AND PREDICTS A GENERAL INCREASE IN DISEASE PREVALENCE, Journal of Medical Genetics, 32(2), 1995, pp. 142-142
MUTATIONAL BIAS PROVIDES A MODEL FOR THE EVOLUTION OF HUNTINGTONS-DISEASE AND PREDICTS A GENERAL INCREASE IN DISEASE PREVALENCE
Authors: RUBINSZTEIN DC AMOS W LEGGO J GOODBURN S RAMESAR RS OLD J BONTROP R MCMAHON R BARTON DE FERGUSONSMITH MA
Citation: Dc. Rubinsztein et al., MUTATIONAL BIAS PROVIDES A MODEL FOR THE EVOLUTION OF HUNTINGTONS-DISEASE AND PREDICTS A GENERAL INCREASE IN DISEASE PREVALENCE, Nature genetics, 7(4), 1994, pp. 525-530
THE ORIGIN OF THE BETA-THALASSEMIA MUTATIONS IN THE UNITED-ARAB-EMIRATES (UAE)
Authors: OLD J QUAIFE R FITCHES A VALLER D ABBES S FITZGERALD P ALGAZALI L THEIN S DAAR S
Citation: J. Old et al., THE ORIGIN OF THE BETA-THALASSEMIA MUTATIONS IN THE UNITED-ARAB-EMIRATES (UAE), Journal of Medical Genetics, 31(2), 1994, pp. 165-166
EFFECT OF ALPHA-THALASSEMIA TRAIT AND ENHANCED GAMMA-CHAIN PRODUCTIONON DISEASE SEVERITY IN BETA-THALASSEMIA MAJOR AND INTERMEDIA
Authors: GRINGRAS P WONKE B OLD J FITCHES A VALLER D KUAN AM HOFFBRAND V
Citation: P. Gringras et al., EFFECT OF ALPHA-THALASSEMIA TRAIT AND ENHANCED GAMMA-CHAIN PRODUCTIONON DISEASE SEVERITY IN BETA-THALASSEMIA MAJOR AND INTERMEDIA, Archives of Disease in Childhood, 70(1), 1994, pp. 30-34
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