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1دورية أكاديمية
مصطلحات موضوعية: Homozygote, Polymorphism, Single Nucleotide - genetics, RNA, Messenger - blood - genetics, Receptors, Transferrin - deficiency - genetics, Reverse Transcriptase Polymerase Chain Reaction, alpha-Thalassemia - complications - genetics, Heterozygote, Hemochromatosis - complications - genetics, Gene Frequency, DNA Mutational Analysis, Alleles, China, Histocompatibility Antigens Class I - genetics, Humans, Iron Overload - blood - etiology - genetics, Membrane Proteins - genetics, Point Mutation - genetics
العلاقة: Blood Cells, Molecules, and Diseases; http://www.scopus.com/mlt/select.url?eid=2-s2.0-0037232545&selection=ref&src=s&origin=recordpageTest; Blood Cells, Molecules, And Diseases, 2003, v. 30 n. 1, p. 107-111; 111; 80504; WOS:000182182200012; http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1079-9796&volume=30&spage=107&epage=111&date=2003&atitle=Can+Defects+in+Transferrin+Receptor+2+and+Hereditary+Hemochromatosis+Genes+Account+for+Iron+Overload+in+HbH+DiseaseTest?+; eid_2-s2.0-0037232545; 107; http://hdl.handle.net/10722/78003Test; 30
الإتاحة: https://doi.org/10.1016/S1079-9796Test(03)00013-5
http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1079-9796&volume=30&spage=107&epage=111&date=2003&atitle=Can+Defects+in+Transferrin+Receptor+2+and+Hereditary+Hemochromatosis+Genes+Account+for+Iron+Overload+in+HbH+DiseaseTest?+
http://hdl.handle.net/10722/78003Test -
2دورية أكاديمية
المؤلفون: Srivastava, G, Liang, RHS, Au, WY, Chen, YW, Wong, KY
مصطلحات موضوعية: Base Sequence, Dna Primers, Exons, Heterozygote, Homozygote, Humans, Lymphoma - Genetics - Pathology, Lymphoma, B-Cell, Marginal Zone - Genetics - Pathology, Mutation, Neoplasm Proteins - Genetics, Polymerase Chain Reaction, Polymorphism, Genetic, Stomach Neoplasms - Genetics - Pathology, Adaptor Proteins, Signal Transducing
العلاقة: Cancer Genetics and Cytogenetics; http://www.scopus.com/mlt/select.url?eid=2-s2.0-0034968228&selection=ref&src=s&origin=recordpageTest; Cancer Genetics And Cytogenetics, 2001, v. 127 n. 2, p. 184-187; 187; 59737; WOS:000169473600015; eid_2-s2.0-0034968228; 184; http://hdl.handle.net/10722/148226Test; 127
الإتاحة: https://doi.org/10.1016/S0165-4608Test(00)00442-8
http://hdl.handle.net/10722/148226Test -
3دورية أكاديمية
مصطلحات موضوعية: thalassemia, cerebrovascular disorders, cerebral infarction, Intracranial Embolism and Thrombosis/*complications/radiography, Humans, Heterozygote, Hemoglobins, Abnormal/genetics, Hemoglobin E/genetics, Female, Child, Cerebral Infarction/etiology, Tomography, X-Ray Computed, Thalassemia/*complications/genetics, Male, Adult, Brain/radiography, Carotid Arteries/radiography, Cerebral Angiography
العلاقة: Stroke; Stroke, 1990, v. 21 n. 5, p. 812-816; 816; WOS:A1990DD82900020; 2339462; eid_2-s2.0-0025334710; 812; http://hdl.handle.net/10722/143501Test; 21