Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.
Huang CH, Chen Y, Reid ME, Seidl C.
Blood. 1998 Jul 15;92(2):664-71.
[RHnull disease].
Hrubisko M, Fábryová L, Lipsic T.
Vnitr Lek. 1974 Jul;20(6):555-62.
Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment.
Huang CH, Liu Z, Cheng G, Chen Y.
Blood. 1998 Sep 1;92(5):1776-84.
Phosphatidylserine transport in Rhnull erythrocytes.
Smith RE, Daleke DL.
Blood. 1990 Sep 1;76(5):1021-7.
Identification of a cell-surface antigen produced by a gene on human chromosome 3 (cen-q22) and not expressed by Rhnull cells.
Miller YE, Daniels GL, Jones C, Palmer DK.
Am J Hum Genet. 1987 Dec;41(6):1061-70.
Rhnull syndrome: identification of a novel mutation in RHce.
Rosa KA, Reid ME, Lomas-Francis C, Powell VI, Costa FF, Stinghen ST, Watanabe AM, Carboni EK, Baldon JP, Jucksch MM, Castilho L.
Transfusion. 2005 Nov;45(11):1796-8. doi: 10.1111/j.1537-2995.2005.00605.x.
Structure and expression of the RH locus in the Rh-deficiency syndrome.
Chérif-Zahar B, Raynal V, Le Van Kim C, D'Ambrosio AM, Bailly P, Cartron JP, Colin Y.
Blood. 1993 Jul 15;82(2):656-62.
Rhnull red cells and pregnancy.
Gibbs BJ, Moores P.
Vox Sang. 1983;45(1):83-6. doi: 10.1111/j.1423-0410.1983.tb04127.x.
Biological functions of blood groups in health and disease.
Sandler SG, Mallory D.
Haematologia (Budap). 1995;27(1):1-13.
Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.
Silvy M, Beley S, Peyrard T, Ouchari M, Abdelkefi S, Jemni Yacoub S, Chiaroni J, Bailly P.
Transfusion. 2015 Jun;55(6 Pt 2):1407-10. doi: 10.1111/trf.12937. Epub 2014 Nov 21.
