| scholarly article | Q13442814 |
| P50 | author | Jacques Chiaroni | Q30353520 |
| P2093 | author name string | Monique Silvy | |
| Pascal Bailly | |||
| Saloua Jemni-Yacoub | |||
| Narjes Kacem | |||
| P2860 | cites work | Management of Rhesus Alloimmunization in Pregnancy | Q22242754 |
| A simple salting out procedure for extracting DNA from human nucleated cells | Q27861086 | ||
| RHD gene deletion occurred in the Rhesus box. | Q33905070 | ||
| Molecular determination of RHD zygosity:predicting risk of hemolytic disease of the fetus and newborn related to anti‐D | Q34149450 | ||
| A new fetal RHD genotyping test: costs and benefits of mass testing to target antenatal anti-D prophylaxis in England and Wales | Q34556245 | ||
| Management and prevention of red cell alloimmunization in pregnancy: a systematic review | Q38054551 | ||
| RHD zygosity assignments based on most probable genotype and hybrid Rhesus box detection in Tunisia | Q39114584 | ||
| Fetal RhD genotyping by real time quantitative PCR in maternal plasma of RhD-negative pregnant women from the Sahel of Tunisia | Q39276151 | ||
| Molecular background of D-negative phenotype in the Tunisian population | Q39276156 | ||
| Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service | Q40626763 | ||
| Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis | Q45053141 | ||
| Evaluation of single-nucleotide polymorphisms as internal controls in prenatal diagnosis of fetal blood groups. | Q45984957 | ||
| Molecular analysis of inactive and active RHD alleles in native Congolese cohorts | Q46180683 | ||
| Molecular characterization of a new D- - haplotype in a Comorian man. | Q46301426 | ||
| The highly variable RH locus in nonwhite persons hampers RHD zygosity determination but yields more insight into RH-related evolutionary events | Q46529462 | ||
| RHCE*cE734C allele encodes an altered c antigen and a suppressed E antigen not detected with standard reagents. | Q50504020 | ||
| Genetic mechanisms of Rhesus box variation. | Q54676826 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| Frequency of partial D phenotypes in the south western region of France | Q71812598 | ||
| Testing for the D zygosity with three different methods revealed altered Rhesus boxes and a new weak D type | Q73215531 | ||
| PCR screening for common weak D types shows different distributions in three Central European populations | Q73402673 | ||
| Prenatal diagnosis of the Rhesus D fetal blood type on amniotic fluid in daily practice | Q80800757 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 59-65 | |
| P577 | publication date | 2014-06-19 | |
| P1433 | published in | Blood transfusion = Trasfusione del sangue | Q26842792 |
| P1476 | title | Paternal RHD zygosity determination in Tunisians: evaluation of three molecular tests | |
| P478 | volume | 13 |
| Q90232580 | A proposal for a rational transfusion strategy in patients of European and North African descent with weak D type 4.0 and 4.1 phenotypes |
| Q53682461 | A proposal for a rational transfusion strategy in patients of European and North African descent with weak D type 4.0 and 4.1 phenotypes. |
| Q92087106 | RHD Genotyping by Molecular Analysis of Hybrid Rhesus box in RhD-Negative Blood Donors from Iran |
| Q46442270 | Transfusion strategy for weak D Type 4.0 based on RHD alleles and RH haplotypes in Tunisia. |
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