Single-cell analysis of the RhD blood type for use in preimplantation diagnosis in the prevention of severe hemolytic disease of the newborn
- 28 February 1995
- journal article
- Published by Elsevier in American Journal of Obstetrics and Gynecology
- Vol. 172 (2), 533-540
- https://doi.org/10.1016/0002-9378(95)90569-3
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Molecular genetic basis of the human Rhesus blood group systemNature Genetics, 1993
- Multiple Rh messenger RNA isoforms are produced by alternative splicingBlood, 1992
- Assignment of the chromosomal locus of the human 30-kDal Rh (Rhesus) blood group-antigen-related protein (Rh30A) to chromosome region 1p36.13→p34Cytogenetic and Genome Research, 1992
- Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysisBlood, 1991
- Enhanced sensitization after cordocentesis in a rhesus-isoimmunized pregnancyAmerican Journal of Obstetrics and Gynecology, 1991
- Molecular biology of the Rh antigensBlood, 1991
- Localization of the human Rh blood group gene structure to chromosome region 1p34.3–1p36.1 by in situ hybridizationHuman Genetics, 1991
- cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expressionBiochemical Journal, 1990
- Failures of Intravenous Rh Immune Globulin Prophylaxis: An Analysis of the Reasons for Such FailuresTransfusion Medicine Reviews, 1987
- Ultrasound-guided fetal intravenous transfusion for severe rhesus haemolytic disease.BMJ, 1982