微缺失

A microdeletion was identified on chromosome 16 in the patient, causing developmental delays.
这个句子的意思是：在患者的第16号染色体上发现了一个微缺失，导致了发育迟缓。
The genetic counselor informed the family that their child had a microdeletion on the short arm of chromosome 3, affecting language development.
遗传顾问告诉家庭，他们的孩子在3号染色体短臂上有一个微缺失，影响了语言发展。
Researchers found a rare microdeletion in the DNA sequence, which could explain the unique traits observed in the individual.
研究人员在DNA序列中发现了一种罕见的微缺失，这可能解释了个体的独特特征。
The microdeletion was detected through a high-resolution comparative genomic hybridization (CGH) analysis.
通过高分辨率的比较基因组杂交（CGH）分析，发现了微缺失。
In some cases, microdeletions can be inherited from a parent, while in others, they arise spontaneously during fetal development.
有时，微缺失可以从父母那里遗传，而在其他情况下，它们是在胎儿发育过程中自发产生的。
Early intervention programs were recommended for children with microdeletions to address the associated learning difficulties.
建议对有微缺失的儿童进行早期干预，以应对相关的学习困难。
Scientists have linked certain microdeletions to specific neurological disorders, such as autism spectrum disorder (ASD).
科学家已经将某些微缺失与特定的神经系统疾病联系起来，如自闭症谱系障碍（ASD）。
Genetic testing revealed that the couple's baby had a microdeletion on the X chromosome, resulting in a condition known as Turner syndrome.
基因检测显示，这对夫妇的孩子在X染色体上有微缺失，导致了特纳综合症。
The study investigated the prevalence and impact of microdeletions in a large population, providing valuable insights into genetic variation.
这项研究调查了大样本中微缺失的普遍性和影响，提供了关于遗传变异的重要见解。
Detecting microdeletions accurately is crucial for proper diagnosis and personalized treatment planning for affected individuals.
准确检测微缺失对于受影响个体的正确诊断和个性化治疗计划至关重要。