结果16号染色体短臂的平均杂合缺失率为24.58%，仅有一高频缺失位点d 16s404，杂合缺失率达52.73%。
Results the average LOH frequency of chromosome 16p was 24. 58%, the highest LOH ratio was found at D16S404 (52. 73%).
在另一次音乐品味的缺失中，一位患病的妇女突然开始创作并演唱乡村和西部歌曲。
In another lapse of musical taste, one woman with the disease suddenly started composing and singing country and western songs.
一位由于大脑某个结构缺失而无法感受到恐惧的妇女，可能为科学家发现创伤后应激障碍(PTSD)治疗方法带来帮助。
A woman who cannot feel afraid because of a missing structure in her brain could help scientists discover treatments for post-traumatic stress disorder (PTSD).
一份对英国4500位女性的长期研究发现，在婴儿期没有接受母乳喂养，在成长中缺失父爱的女孩很容易成为少年妈妈。
Girls who are not breastfed as babies or who grow up without a father are likely to have their own children earlier, according to a long-term study of more than 4,500 women across the UK.
一位专家接受BBC采访时表示，这种隐私设置的缺失是一个问题。
One expert told the BBC the lack of privacy settings was a concern.
他自己也是一位艺术家，作为音乐指导和美国管弦交响乐指挥的他，曾经谴责过大学对于塑造完整公民义务的缺失。
Dr. Botstein has accused colleges of shirking their responsibility to create a well-rounded citizenry.
在这个以缺失主语的句子为命名的展览里，我们将呈现四位风格迥异的日本与中国当代艺术家新作。
In this exhibition, without subject name, you will see four up-to-date style works of art produced by Chinese and Japanese contemporary artists.
但如果我们开诚不公，就会承认还有太多的父亲不在其位——在太多孩子的生活里，在太多的家庭里，父亲的这一角色是缺失的。
But if we open and injustice, will not admit too many fathers in their place...... too many children's lives where, in too many families, the father of this role is missing.
该序列一共具有34个分析性状（包括17个变异位点，9个位点碱基缺失）。
There were 34 analyzing characters could be used for analysis, including 17 transpositional loci and 9 missing ones.
“德国缺失的是它的领导力量而不是旁观巴黎和伦敦编造了什么”，一位北约的外交官说。
"What's missing is Germany leading rather than seeing what Paris and London cook up," says a NATO diplomat.
并通过对患者家庭进行分析确定标记位点缺失的遗传学来源。
Linkage analyses were also performed to identify the parental origin of deletion.
方法：采用PCR及微卫星多态性技术，对65例肝癌1号染色体上28个微卫星标志位点杂合性缺失进行检测。
Methods: LoH of chromosome 1 were detected by PCR based microsatellite polymorphism analysis technique using 28 pairs of microsatellite markers primers in 65 HCC.
右位心胎儿DV多普勒血流波形的心房收缩波近缺失。
DV Doppler waveform of this dextrocardia fetus showed a nearly ab - sent atrial systole wave.
目的用先天性缺牙编码(TAC)及传统缺失牙位方式比较先天缺牙表型及基因型的相关性。
Objective to analyze the correlation between the phenotype and genotype of tooth agenesis using the tooth agenesis code (TAC) and the traditional descriptor for missing teeth.
结论3例FA-A型患者均无功能性FANCA蛋白表达；基因缺失、移码突变和剪切位点突变是FANCA基因的主要失活方式。
Conclusions No functional FANCA protein was found in these 3 cases of FA-A, and intragenic deletion, frame shift and splice site mutation were the major pathogenic mutations found in FANCA gene.
一位学者把它描述成“意思是没有自我，区分自我和众人及其它事物的个人特性的缺失。”
One scholar describes it as "meaning non-selfhood, the absence of limiting self- identity in people and things."
一位学者把它描述成“意思是没有自我，区分自我和众人及其它事物的个人特性的缺失。”
One scholar describes it as "meaning non-selfhood, the absence of limiting self- identity in people and things."
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