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January 1, 1994Annals of Human Genetics34 citations

Lack of RH C/E expression in the Rhesus D– phenotype is the result of a gene deletion

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TBT BluntFSF. STEERSGDGeoff Daniels

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Abstract

We have investigated the arrangement of genes in the rare Rh (Rhesus) partial null condition D--. Southern blot and PCR studies under conditions which distinguish the highly homologous RH D and RH C/E genes show that in an Icelandic family with the D-- haplotype at least 85% of the RH C/E gene is deleted. This finding is in contrast to one other published case of this phenotype, where intact RH D and C/E genes were found, and also to the full amorph Rhnull phenotype, where an intact RH C/E gene was found, accompanied by the deletion of the RH D gene typical of Rh D-negative individuals.

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Cite This Study

Blunt et al. (1994) studied this question.

synapsesocial.com/papers/6a97231317cb0e8b160e41c3https://doi.org/10.1111/j.1469-1809.1994.tb00722.x
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Rh null phenotypes are not due to a gross deletion and can occure on different Rh genetic backgrounds1993 · 21 citations
  2. 2Molecular cloning and primary structure of the human blood group RhD polypeptide.1992 · 311 citations
  3. 3Molecular cloning of RhD cDNA derived from a gene present in RhD- positive, but not RhD-negative individuals1993 · 205 citations
  4. 4A speculative model for the Rh blood groups1986 · 64 citations
  5. 5Sequences homologous to the human D1S1 locus present on human chromosome 3.1986 · 60 citations