| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Reid ME | |
| P2860 | cites work | Molecular defects underlying the Kell null phenotype | Q40803254 |
| Insights into the structure and function of membrane polypeptides carrying blood group antigens | Q40846483 | ||
| Production and characterization of anti-kell monoclonal antibodies using transfected cells as the immunogen | Q40932158 | ||
| 16Cys encoded by the RHce gene is associated with altered expression of the e antigen and is frequent in the R0 haplotype | Q43622739 | ||
| DNA analysis for the Dombrock polymorphism | Q43734112 | ||
| Detection of microchimerism by PCR is a function of amplification strategy | Q45234240 | ||
| Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety | Q46315815 | ||
| Molecular identification of Knops blood group polymorphisms found in long homologous region D of complement receptor 1. | Q47882103 | ||
| Reference typing report for complement receptor 1 (CR1). | Q48763711 | ||
| Cloning and regulation of the ABO genes | Q48768209 | ||
| Rhesus D typing | Q49277361 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| The molecular genetics of the human I locus and molecular background explain the partial association of the adult i phenotype with congenital cataracts | Q24317368 | ||
| Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum | Q24567463 | ||
| Identification of fetal DNA and cells in skin lesions from women with systemic sclerosis | Q28268533 | ||
| Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma | Q28314918 | ||
| [21] Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction | Q29544077 | ||
| Genotyping fetal DNA by non-invasive means: extraction from maternal plasma | Q31920253 | ||
| Red cell antigens on band 3 and glycophorin A. | Q33915284 | ||
| Molecular basis for the p phenotype. Identification of distinct and multiple mutations in the alpha 1,4-galactosyltransferase gene in Swedish and Japanese individuals | Q33918202 | ||
| Polymerase chain reaction with sequence-specific primers-based genotyping of the human Dombrock blood group DO1 and DO2 alleles and the DO gene frequencies in Chinese blood donors | Q34087991 | ||
| Insights into the Holley- and Joseph- phenotypes | Q34118686 | ||
| Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene | Q34129677 | ||
| Scianna antigens including Rd are expressed by ERMAP. | Q34155732 | ||
| Microarray technology: the future of blood testing? | Q34242406 | ||
| DNA chips: a new tool for genetic analysis and diagnostics | Q34333887 | ||
| Fetal DNA in maternal plasma: application to non-invasive blood group genotyping of the fetus | Q34333910 | ||
| Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. | Q34385131 | ||
| Female alloimmunization with antibodies known to cause hemolytic disease | Q34414953 | ||
| Characterization of the gene encoding the human Kidd blood group/urea transporter protein. Evidence for splice site mutations in Jknull individuals | Q34467692 | ||
| P433 | issue | 12 | |
| P304 | page(s) | 1748-1757 | |
| P577 | publication date | 2003-12-01 | |
| P1433 | published in | Transfusion | Q15758500 |
| P1476 | title | Applications of DNA-based assays in blood group antigen and antibody identification | |
| P478 | volume | 43 |
| Q41407564 | ABO, D blood typing and subtyping using plug-based microfluidics |
| Q35915095 | Alternative blood products and clinical needs in transfusion medicine |
| Q42530509 | Applications and Experience with PCR-Based Assays to Predict Blood Group Antigens |
| Q46475678 | Blood group genotype analysis for the quality improvement of reagent test red blood cells |
| Q41186786 | Blood group polymorphisms in Brazil |
| Q43131903 | Comment on "Applying molecular immunohaematology to regularly transfused thalassaemic patients in Thailand". |
| Q37764940 | Detection of blood-transmissible agents: can screening be miniaturized? |
| Q50701292 | Determination of 24 minor red blood cell antigens for more than 2000 blood donors by high-throughput DNA analysis. |
| Q92381730 | Evaluation of molecular typing and serological methods in solving discrepant results of weak and partial D (Rh) in South Egypt |
| Q37315703 | External quality assessment in molecular immunohematology: the INSTAND proficiency test program |
| Q51303498 | Genotyping of the Kidd blood group with allele-specific oligodeoxynucleotides coupled to fluorescent microspheres. |
| Q34590286 | Molecular genetics and clinical applications for RH. |
| Q36431137 | Molecular genetics of RH and its clinical application |
| Q36874235 | New technologies in immunohaematology |
| Q36861105 | Overview of molecular methods in immunohematology |
| Q90761805 | Predicted S and s phenotypes from genotyping results among Thai populations to prevent transfusion-induced alloimmunization risks |
| Q50534685 | Prevalence of erythrocyte alloimmunization in polytransfused patients. |
| Q40896110 | Red blood cell antigen genotype analysis for 9087 Asian, Asian American, and Native American blood donors |
| Q36861142 | Red blood cell antigen phenotype by DNA analysis |
| Q39666681 | Screening for the SMIM1*64_80 del Allele in blood donors in a population from Southern Brazil |
| Q34306073 | Sequence-Based Typing of Human Blood Groups |
| Q39089395 | Serologic findings of RhD alleles in Egyptians and their clinical implications |
| Q40219602 | Small world - advance of microarrays: current status and future trends |
| Q34006112 | Transfusion in the age of molecular diagnostics |
| Q39089407 | Weak D types in the Egyptian population |
| Q80390999 | [Future technological evolutions in blood donation qualification] |
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