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A weak D type 59 case identified in the Chinese Han population / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 261-264, 2018.
Article in Chinese | WPRIM | ID: wpr-687964
ABSTRACT
<p><b>OBJECTIVE</b>To study a case with weak D59 phenotype identified among ethnic Han Chinese population.</p><p><b>METHODS</b>Routine serological tests were used to analyze the reaction patterns, and the RhD epitopes were verified with 12 monoclonal antibodies. Sequence-specific primer PCR was applied for typing the weak RhD and RhD zygosity in the proband and his family members.</p><p><b>RESULTS</b>A c.1148T>C variant was identified in the proband, for which serological test indicated a weak D phenotype. RHD zygosity testing confirmed that the proband had a RHD+ /RHD- genotype.</p><p><b>CONCLUSION</b>A weak D59 phenotype was firstly identified in a Chinese individual.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / Rh-Hr Blood-Group System / China / Asian People / Ethnology / Genetics Type of study: Prognostic study Limits: Humans / Male Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2018 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Phenotype / Rh-Hr Blood-Group System / China / Asian People / Ethnology / Genetics Type of study: Prognostic study Limits: Humans / Male Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2018 Type: Article