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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.
Artículo en Chino | 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>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fenotipo / Sistema del Grupo Sanguíneo Rh-Hr / China / Pueblo Asiatico / Etnología / Genética Tipo de estudio: Estudio pronóstico Límite: Humanos / Masculino País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2018 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Fenotipo / Sistema del Grupo Sanguíneo Rh-Hr / China / Pueblo Asiatico / Etnología / Genética Tipo de estudio: Estudio pronóstico Límite: Humanos / Masculino País/Región como asunto: Asia Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2018 Tipo del documento: Artículo