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pedigrees相关的网络例句

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与 pedigrees 相关的网络例句 [注:此内容来源于网络,仅供参考]

Results Every member of the 4 pedigrees was examined genetically. Besides the 4 probands, another 1 homozygote and 8 heterozygotes were found.

结果 各家系成员均从基因水平明确了诊断,23例个体中,除先证者外,还发现1例纯合子,8例杂合子。

Objective To investigate the gene mutation in two pedigrees with X-linked ichthyosis and explore the relationship between the mutation and clinical manifestations.

目的 研究X性连锁遗传鱼鳞病家系基因突变,探讨基因突变与临床表现的关系,为进一步开展基因诊断和基因治疗奠定基础。

Objective To study the genetic characteristics of keloid in 6 Chinese Han pedigrees.

目的 研究中国汉族瘢痕疙瘩家系的遗传学特征。

That is why it is essential to study the pedigrees of your mating pair.

这就是为什么对于交配犬只血统的了解是如此的重要。

Northumbrian Type 诺斯安布赖恩类型 Almost all present-day Border Collies can trace their pedigrees back to a dog known as Old Hemp.

追溯几乎目前所有的边境牧羊犬的血统都集中到一只叫Old Hemp的狗。1894年住在英格兰Northumbrian地区的名为Adam Telfer的人繁育出了Hemp,并一直养育着他。

MAIN OUTCOME MEASURES: Log of the odds at each locus when the penetrance of NM and LN keloid pedigrees was 90%.

主要观察指标:NM和LN瘢痕疙瘩家系外显率为90%时各位点LOD值。

Five pedigrees with high incidence of schizophrenia were studied by polymerize chain reaction and restriction fragment length polymorphism technique.

应用聚合酶链反应和限制性片段长度多态性方法对5个精神分裂症高发家系进行初步研究。

My own study of standard poodle pedigrees is consistent with the interpretation that grey and silver are separate genes.

通过我自己的学习贵宾的标准及解释,我认为灰色和银色是不同的基因。

Based on the number of families with at least one affected girl and the number of patients per sibship among these pedigrees, the proportion of families with DMD inherited as an AR trait was estimated.

结果:常染色体隐性遗传的类DMD患者独立行走的平均时间为(1.47±1.00)岁,症状出现的平均时间为(8.11±4.32)岁,血清肌酸激酶平均水平为(2785.10±1500.29)U/L,这种常染色体隐性遗传型类DMD占DMD的9.4%。

Gene diagnosis and functional study were conducted in different pedigrees of inherited hemorrhagic and thrombotic diseases including 21 of rare coagulation factor deficiencies, 2 of Glanzmann thrombasthenia, 2 of hereditary hemorrhagic telangiectasis, 13 of AT deficiency, 16 of PC deficiency, 3 of PS deficiency and 2 of combined PC/PS deficiency.

遗传性出血病方面,对21个少见的遗传性凝血因子缺陷症家系、2个血小板无力症家系、2个出血性毛细血管扩张症家系进行了相关基因与功能的研究。遗传性血栓病方面,对13个AT缺陷家系、16个PC缺陷家系、3个PS缺陷家系和2个PC/PS联合缺陷家系进行了相关基因诊断与功能的研究。

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从有历史以来,英国,在此地早期居住的是凯尔特人,已经被征服了三次。

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