A Rare RhD-Phenotype Caused by Gene RHCE-D (1-9)-CE (10)

被引:0
|
作者
Huang, Zhen [1 ]
Zhu, Zhe [1 ]
Zhu, Shasha [1 ]
机构
[1] Ningbo 2 Hosp, Dept Transfus, Ningbo, Peoples R China
关键词
D O I
10.1007/s12288-023-01720-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:362 / 363
页数:2
相关论文
共 42 条
  • [21] Breakpoint Regions of an RHD-CE(4-9)-D Allele Expressing a C Antigen and a Rare JK Allele in a Pacific Islander Individual
    Srivastava, K.
    Bueno, M.
    Flegel, W.
    TRANSFUSION, 2023, 63 : 177A - 178A
  • [22] 携带RhD-CE(2-9)-D基因并检出高效价同种抗-D抗体1例报告
    周毓菁
    王雪明
    袁异玮
    蒋敏
    顾国浩
    李勇
    张健
    郑元
    临床检验杂志, 2012, 30 (05) : 397 - 397
  • [23] Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles (vol 52, pg 759, 2012)
    Fichou, Y.
    Le Marechal, C.
    Bryckaert, L.
    Guerry, C.
    Benech, C.
    Dupont, I
    Jamet, D.
    Ferec, C.
    Chen, J-M
    TRANSFUSION, 2012, 52 (08) : 1842 - 1842
  • [24] Severe XLP Phenotype Caused by a Novel Intronic Mutation in the SH2D1A Gene
    B. Tóth
    B. Soltész
    E. Gyimesi
    G. Csorba
    Á. Veres
    Á. Lányi
    G. Kovács
    L. Maródi
    M. Erdős
    Journal of Clinical Immunology, 2015, 35 : 26 - 31
  • [25] Severe XLP Phenotype Caused by a Novel Intronic Mutation in the SH2D1A Gene
    Toth, B.
    Soltesz, B.
    Gyimesi, E.
    Csorba, G.
    Veres, A.
    Lanyi, A.
    Kovacs, G.
    Marodi, L.
    Erdoes, M.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2015, 35 (01) : 26 - 31
  • [26] Identification of a novel variant (c.1-111A>G) located in GATA-1 motif of RHCE proximal promoter in two Chinese patients with the rare D-- phenotype
    Zhang, Ran
    Wen, Jizhi
    Tang, Changjiu
    Jia, Shuangshuang
    Chen, Qi
    Ji, Yanli
    TRANSFUSION, 2025,
  • [27] A D plus blood donor with a novel RHD*D-CE(5-6)-D gene variant exhibits the low-frequency antigen RH23 (DW) characteristic of the partial DVa phenotype
    Lopez, Genghis H.
    McGowan, Eunike C.
    McGrath, Kelli A.
    Abaca-Cleopas, Maria E.
    Schoeman, Elizna M.
    Millard, Glenda M.
    O'Brien, Helen
    Liew, Yew-Wah
    Flower, Robert L.
    Hyland, Catherine A.
    TRANSFUSION, 2016, 56 (09) : 2322 - 2330
  • [28] 1例RHD-CE(3-7)-D基因重组与RHCE变异型患者的血清学与分子生物学分析
    唐炳娣
    蔡仲仁
    邓泳诗
    伍昌林
    分子诊断与治疗杂志, 2024, 16 (06) : 1183 - 1186+1190
  • [29] EAST syndrome - expanding the clinical phenotype of this recently delineated, rare autosomal recessive multisystemic disorder caused by mutations in the potassium channel gene KCNJ10
    Prapa, M.
    Parker, A.
    Brown, R.
    Carss, K.
    Spasic-Boskovic, O.
    Twiss, P.
    Brugger, K.
    Martin, H.
    Abbs, S.
    Raymond, L. F.
    Park, S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 467 - 467
  • [30] SUBCUTANEOUS AND INTRANASAL USE OF D-SER (TBU)6 LHRH 1-9 EA10 (HOE-766) IN PRECOCIOUS PUBERTY (PP)
    HOLLAND, J
    FISHMAN, L
    COSTIGAN, DC
    WIELGOSZ, G
    FAZEKAS, A
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1984, 20 (6B): : 1380 - 1380