X-linked的例句大全

Two main modes of inheritance exist: X-linked and autosomal dominant.

本病存在两种主要的遗传方式: X - 连锁型和常染色体显性型.

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The inheritance pattern of EDMD includes X-linked recessive, autosomal dominant and recessive modes.

其遗传方式为X - 连锁隐性 、 染色体显性和隐性遗传.

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Analysis of pedigrees however has indicated that it may be also inherited as an X-linked trait.

系谱的分析表明了它有可能 X 相关特征遗传的.

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Objective : To investigate the possibility of X-linked dominant genetic model in unipolar depression.

目的: 探讨单相抑郁症 X 连锁显性遗传方式的可能性.

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Breeders need to be aware of the sex linked diseases, which is an abnormal gene contained in X chromosome.

繁殖者需要了解到的性状疾病，那就是X染色体中存在着不正常的基因。

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Family investigation result in, X-Chromosom sex linked inheritance dominant in 1 cases, Rarely inheritance recessive in 3 cases ( autosomal recessive inheritance in 2 case, X-chromosom sex linked recessive inheritance in 1 case), no report in china.

家系调查结果：显性遗传1例，稀有的隐性遗传3例，国内尚未见报导。

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Clinical and genetic analysis of 10 cases with X-linked agammaglobulinemia

10例X连锁无丙种球蛋白血症的临床分析和基因诊断

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X-linked agammaglobulinemia: a case report and literature review

X-连锁无丙种球蛋白血症1例

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X-linked agammaglobulinemia: a case report and literature review Gene diagnosis of X-linked agammaglobulinemia

X连锁无丙种球蛋白血症的基因诊断X-连锁无丙种球蛋白血症一例报告及文献复习

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Conclusion This is the first case report of successful treatment of X-linked agammaglobulinemia by HLA-mismatched unrelated CBT.

结论本例为首例非血缘CBT治疗Bruton病获得成功；HLA不全相合非血缘CBT治疗非恶性血液病安全、有效。

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Objective To appraise the clinical features, diagnosis and treatment of juvenile idiopathic arthritis ( JIA) with X Linked Agammaglobulinemia ( XLA).

目的探讨X连锁无丙种球蛋白血症（XLA）合并幼年特发性关节炎（JIA）的临床表现、诊断和治疗的特点。

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Objective To evaluate cord blood stem cell transplantation ( CBT) in the treatment of X-linked agammaglobulinemia, and observe the courses of the hematopoietic and immune reconstitution.

目的探讨HLA不全相合非血缘脐血移植（CBT）治疗X连锁无丙种球蛋白血症（Bruton病）的疗效；观察其造血及免疫重建过程。

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Results The clinical diagnosis of the case was X-Linked Agammaglobulinemia and fell into the category of immunodeficient vaccine-derived poliovirus case through classified diagnosis which was the first finding in China.

结果病例临床诊断为X-连锁低/无丙种球蛋白血症，最终分类诊断为免疫缺陷疫苗衍生脊灰病毒病例，属中国首例。

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