physicians diagnose various haemoglobinemias through comprehensive blood analysis.
医生通过全面的血液分析诊断各种血红蛋白病。
the laboratory is researching the genetic causes of inherited haemoglobinemias.
实验室正在研究遗传性血红蛋白病的遗传原因。
common haemoglobinemias often present with symptoms of severe anemia.
常见的血红蛋白病通常表现为严重贫血的症状。
pathologists identify several distinct types of haemoglobinemias in newborns.
病理学家在新生儿中识别出几种不同类型的血红蛋白病。
advanced treatments for haemoglobinemias have improved patient survival rates.
先进的血红蛋白病治疗方法提高了患者的生存率。
detecting abnormal haemoglobinemias requires specialized electrophoresis testing equipment.
检测异常血红蛋白病需要专用的电泳检测设备。
some haemoglobinemias result from specific genetic point mutations.
一些血红蛋白病是由特定的基因点突变引起的。
the medical journal published a review on rare haemoglobinemias.
医学期刊发表了一篇关于罕见血红蛋白病的综述。
pediatricians must screen infants for serious haemoglobinemias early.
儿科医生必须早期筛查婴儿是否患有严重的血红蛋白病。
understanding the pathophysiology of haemoglobinemias aids drug development.
了解血红蛋白病的发病机制有助于药物开发。
family history is crucial when diagnosing hereditary haemoglobinemias.
在诊断遗传性血红蛋白病时，家族史至关重要。
physicians diagnose various haemoglobinemias through comprehensive blood analysis.
医生通过全面的血液分析诊断各种血红蛋白病。
the laboratory is researching the genetic causes of inherited haemoglobinemias.
实验室正在研究遗传性血红蛋白病的遗传原因。
common haemoglobinemias often present with symptoms of severe anemia.
常见的血红蛋白病通常表现为严重贫血的症状。
pathologists identify several distinct types of haemoglobinemias in newborns.
病理学家在新生儿中识别出几种不同类型的血红蛋白病。
advanced treatments for haemoglobinemias have improved patient survival rates.
先进的血红蛋白病治疗方法提高了患者的生存率。
detecting abnormal haemoglobinemias requires specialized electrophoresis testing equipment.
检测异常血红蛋白病需要专用的电泳检测设备。
some haemoglobinemias result from specific genetic point mutations.
一些血红蛋白病是由特定的基因点突变引起的。
the medical journal published a review on rare haemoglobinemias.
医学期刊发表了一篇关于罕见血红蛋白病的综述。
pediatricians must screen infants for serious haemoglobinemias early.
儿科医生必须早期筛查婴儿是否患有严重的血红蛋白病。
understanding the pathophysiology of haemoglobinemias aids drug development.
了解血红蛋白病的发病机制有助于药物开发。
family history is crucial when diagnosing hereditary haemoglobinemias.
在诊断遗传性血红蛋白病时，家族史至关重要。
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