X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4668) 4668
Publication (359) 359
Conference Proceeding (22) 22
Book Review (18) 18
Book Chapter (10) 10
Dissertation (5) 5
Book / eBook (2) 2
Journal / eJournal (1) 1
Reference (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (3724) 3724
beta-thalassemia (2082) 2082
beta-thalassemia - genetics (2055) 2055
female (1953) 1953
index medicus (1947) 1947
hematology (1936) 1936
male (1699) 1699
mutation (1388) 1388
adult (1222) 1222
thalassemia (980) 980
biochemistry & molecular biology (809) 809
globins - genetics (749) 749
child (747) 747
beta-thalassemia - diagnosis (729) 729
adolescent (714) 714
heterozygote (582) 582
genotype (576) 576
child, preschool (540) 540
phenotype (529) 529
beta-thalassemia - blood (517) 517
β-thalassemia (512) 512
base sequence (487) 487
beta-globins - genetics (486) 486
hemoglobin (486) 486
pregnancy (486) 486
middle aged (478) 478
mutations (460) 460
genetics & heredity (437) 437
polymerase chain reaction (434) 434
beta-thalassemia - epidemiology (429) 429
dna (427) 427
animals (403) 403
dna mutational analysis (401) 401
anemia (397) 397
alpha-thalassemia (390) 390
prenatal diagnosis (372) 372
prenatal-diagnosis (371) 371
molecular sequence data (362) 362
alleles (356) 356
point mutation (352) 352
beta-thalassemia - therapy (341) 341
young adult (338) 338
alpha-thalassemia - genetics (322) 322
hemoglobins, abnormal - genetics (321) 321
beta-thalassemia - complications (318) 318
diagnosis (317) 317
disease (304) 304
infant (302) 302
prevalence (289) 289
expression (280) 280
gene frequency (275) 275
oncology (269) 269
hemoglobinopathies (264) 264
population (262) 262
gene (261) 261
mice (251) 251
medicine, research & experimental (247) 247
globin gene (244) 244
pedigree (240) 240
homozygote (229) 229
iron overload (225) 225
blood transfusion (222) 222
hemic and lymphatic diseases (220) 220
haplotypes (215) 215
pediatrics (213) 213
anemia, sickle cell - genetics (211) 211
molecular-basis (211) 211
hemoglobinopathies - genetics (209) 209
analysis (207) 207
fetal hemoglobin - genetics (201) 201
beta-thalassemia - metabolism (198) 198
medicine, general & internal (193) 193
thalassemia - genetics (191) 191
medicine & public health (187) 187
intermedia (183) 183
sickle cell disease (183) 183
sickle cell anemia (181) 181
genes (180) 180
genetic aspects (180) 180
iron (179) 179
multidisciplinary sciences (175) 175
mutation - genetics (175) 175
fetal-hemoglobin (174) 174
aged (169) 169
genetics (168) 168
infant, newborn (168) 168
fetal hemoglobin (165) 165
erythropoiesis (162) 162
sickle-cell-disease (161) 161
gene expression (160) 160
genetic testing (159) 159
children (158) 158
research (157) 157
india (156) 156
medical laboratory technology (156) 156
medicine (153) 153
sequence deletion (153) 153
alpha-globins - genetics (152) 152
obstetrics & gynecology (152) 152
prenatal diagnosis - methods (151) 151
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (4496) 4496
Chinese (82) 82
French (24) 24
Spanish (22) 22
Japanese (10) 10
Russian (9) 9
German (8) 8
Portuguese (6) 6
Persian (5) 5
Czech (4) 4
Polish (4) 4
Arabic (2) 2
Danish (2) 2
Dutch (2) 2
Serbian (2) 2
Hebrew (1) 1
Norwegian (1) 1
Slovak (1) 1
Swedish (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Blood Cells, Molecules and Diseases, ISSN 1079-9796, 06/2015, Volume 55, Issue 1, pp. 27 - 29
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 13359 - 14
During cellular division DNA replicates and this process is the basis for passing genetic information to the next generation. However, the DNA copy process... 
TEXT-MINING TOOL | DATABASE | HFE | MULTIDISCIPLINARY SCIENCES | ONTOLOGY | RISK | GENETIC-VARIANTS | GENOME ANNOTATION | BETA-THALASSEMIA | IRON OVERLOAD | HEMOCHROMATOSIS | Data processing | Exploration | Phenotypes | Mutation | Disease | Deoxyribonucleic acid--DNA
Journal Article
BJOG-AN INTERNATIONAL JOURNAL OF OBSTETRICS AND GYNAECOLOGY, ISSN 1470-0328, 03/2018, Volume 125, Issue 4, pp. 461 - 468
ObjectiveTo evaluate whether targeted sequencing and relative mutation dosage can be used to diagnose correctly inheritance of maternal -thalassaemia mutations... 
DIAGNOSIS | thalassaemia | METAANALYSIS | non-invasive prenatal diagnosis | relative mutation dosage | FREE DNA | COLD-PCR | E-BETA-THALASSEMIA | OBSTETRICS & GYNECOLOGY | PLASMA | PREFERENCES | cell-free DNA | MONOGENIC DISEASES | SICKLE-CELL-DISEASE | CYSTIC-FIBROSIS | Gene mutations | Pregnant women
Journal Article
BLOOD, ISSN 0006-4971, 10/2011, Volume 118, Issue 16, pp. 4454 - 4458
Increased hemoglobin A(2) (HbA(2); ie, levels > 3.9%) is the most important feature of beta-thalassemia carriers. However, it is not uncommon to find persons... 
EKLF | FETAL-HEMOGLOBIN | PHENOTYPE | ANEMIA | BETA-THALASSEMIA | IDENTIFICATION | HEMATOLOGY | EXPRESSION | Pedigree | Humans | beta-Thalassemia - genetics | Hemoglobin A2 - metabolism | Erythrocyte Indices | Female | Male | Mutation | beta-Thalassemia - metabolism | Kruppel-Like Transcription Factors - genetics | beta-Thalassemia - diagnosis
Journal Article