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phenylketonuria相关的网络例句

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Objective To investigate the mutation characteristics in exon 7 of the PAH gene in phenylketonuria patients in Xinjiang.

目的研究分析新疆地区苯丙酮尿症患者中苯丙氨酸羟化酶基因外显子7的突变特征。

Other trace elements have been observed with phenylketonuria, an inherited metabolic disorder, and kwashiorkor, a severe form of malnutrition that occurs mainly in developing nations.

在苯丙酮尿症和恶性营养不良(一种主要发生在发展中国家的严重营养不良)患者的毛发中,也观察到了其它种微量元素。

Objective To establish a simple, accurate and rapid method for screening of the mutant genes in phenylketonuria.

目的 建立一种简便、准确和快速的筛查苯丙酮尿症突变基因的方法。

Objective To observe delayed myelination in delayed treated Phenylketonuria with MRI and changes of IQ before and after treatment.

目的 应用磁共振成像观察苯丙酮尿症治疗延迟患儿治疗前后脑髓鞘发育延迟与智商的关系。

Because of its phenylalanine content, persons with phenylketonuria must avoid it.

由于内含苯丙氨酸,患有苯丙酮尿症的人必须避免。

Persons with phenylketonuria do not metabolize phenylalanine properly and must adhere to a diet free of it.

患有苯丙酮尿症的人不能进行苯丙氨酸的正常代谢,必须采取没有苯丙氨酸的饮食方式。

In order to diagnose phenylketonuria early and rapidly for newborns,the fluorescence method for detecting phenylalanine is proposed.

苯丙酮尿症是一种由于人体正常染色体缺陷,造成的新生儿体内苯丙氨酸代谢紊乱性疾病。

Methods Seventy-three patients with clinically and biochemically documented phenylketonuria were studied with use of 0.5 T superconductive MRI.

用0.5 T超导磁共振机对临床检查和生化测定已确诊的73例苯丙酮尿症患儿头颅进行扫描。

This study intends to investigate the essence structure of the family stress experience during the infancy of caretaking classical phenylketonuria children.

本研究运用家庭压力脉络模式,家庭系统思维,探讨患有饮食型苯酮尿症幼儿父母的家庭压力经验之本质结构。

Objective To find out a method that is simple and reliable for screening phenylketonuria heterzygotes.

目的 寻找一种筛查苯丙酮尿症(phenylketonuria, PKU)杂合子的可靠易行方法。

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