英语释义

• any of the diagnostic procedures used to determine whether a fetus has a genetic abnormality

片语

prenatal care产前护理，[妇产] 产前保健；产前检查

prenatal echocardiographic diagnosis产前超声诊断

prenatal genic diagnosis产前基因诊断

Prenatal period diagnosis产前诊断

prenatal molecular diagnosis产前分子诊断

prenatal ultrasonic diagnosis超声产前诊断

prenatal genetic diagnosis产前遗传学诊断

Prenatal Gene Diagnosis产前基因诊断

prenatal early diagnosis早期诊断

prenatal ultrasound diagnosis产前超声诊断

英汉例句

• even if the screening result is positive, you will not necessarily be offered a prenatal diagnosis .

  即使检查结果是积极的，你不一定会提供了产前诊断。

• uk, usa, canada and australia issued the guidelines on inform-consent and explanation for result of diagnosis and standard for prenatal diagnosis services.

  英国、美国、加拿大和澳大利亚都根据各国国情提出了对知情同意、诊断结果解释的指南，制定了相应的服务标準。

• in china, the research on prenatal diagnosis of human genetic diseases has just begun.

  遗传疾病的产前诊断技术在我国才刚刚开展。

• according to the above, standards are established for cdfi to diagnose umbilical cord abnormalities and for non-invasive prenatal diagnosis of fetal distress.

  由此制定了cdfi诊断脐带异常及无创性产前诊断胎儿宫内窘迫的标準。

• objective to discuss the clinical management and significance of the prenatal diagnosis of fetal choroid plexus cysts.

  目的探讨胎儿脉络丛囊肿产前诊断的临床意义及处理原则。

• conclusion amniotic fluid culture for prenatal diagnosis is very safe and reliable.

  结论羊水细胞培养进行产前诊断是十分安全而可靠的。

• fish is a new, effective method for prenatal diagnosis of down's syndrome.

  fish是一种新型产前诊断失天愚型的有效方法。

• studies show medical students are poorly trained about people with disabilities and that some doctors who make a prenatal diagnosis emphasize negative information about the condition, he said.

  研究表明医学学生很少受到有关残障人士知识的培训，许多做孕期检查的医生会强调唐氏综合癥的负面信息。他说。

• objective:to evaluate the role of percutaneous ultrasound-monitored amniocentesis in the prenatal diagnosis of the fetal chromosomal abnormalities.

  目的评价羊水穿刺术在产前诊断胎儿染色体异常中的应用。

• objective to evaluate the safety and clinical value of chorionic villus sampling via the cervix for prenatal diagnosis of early pregnancy.

  目的探讨早孕期经宫颈吸取绒毛术的安全性及临床价值。

• is there any role of ultrasound and invasive test in the post non-invasive prenatal diagnosis era?

  在非入侵性产前诊断的时代，超声及入侵性测试还有何作用?。

• there is a range of findings, including facial abnormalities, that can occur with holoprosencephaly, many of which can be seen in a fetus by ultrasound, so prenatal diagnosis is possible.

  其癥状表现较多，包括面部异常，与前脑无裂畸形同时出现的癥状，可以用超声检测，因此产前诊断是可能的。

• so population screening and prenatal diagnosis are very important measures.

  所以，人群筛选和产前诊断是很重要的措施。

• at the same time, we add new variants to the repertoire of ed1 mutations in xlhed, and that is useful for genetic counselling, carrier detection and prenatal diagnosis in xlhed families.

  结论我们的研究结果提示这两个突变与中国汉族人xlhed的发病有关，同时为突变数据库增加了ed1基因的新的突变位点，为将来的遗传咨询，产前诊断及基因治疗打下基础。

• prenatal ultrasound can provide useful information for prenatal diagnosis of umbilical cord cysts.

  产前超声筛查可提供重要的诊断信息。

• conclusion: our study showed again that the r10 position was hot point for mutation of ehk. it may provide a reliable basis for the prenatal diagnosis and genetic therapy.

  结论：本研究再次表明r10为ehk突变热点，为表皮松解性角化过度疾病的产前诊断和基因治疗奠定了基础。

• prenatal diagnosis is now part of established obstetric practice in many countries.

  目前产前诊断在许多国家是固定的产科检查的一部分。

• abstr act objective to discuss the prenatal diagnosis of birth defects and the intervention measures so as to reduce the incidence.

  目的探讨出生缺陷的产前检查及干预措施，从而降低其发生率。

• the results serve as an evidence for reliable genetic counseling and prenatal diagnosis for this family.

  上述结果是为该家系提供可靠遗传咨询及产前诊断的依据；

• non-invasive prenatal diagnosis of aneuploidies: how close to reality?

  非整倍体异常的非入侵性产前诊断：离现实有多近?。

• the different dna methylation opens up a new way for noninvasive prenatal diagnosis and monitoring .

  孕妇外周血中胎儿游离dna的发现，为无创性产前诊断开辟了一条新途径。

• conclusion this was the first time that cls was diagnosed by molecular method in china, which provided a genetic basis for gene diagnosis and prenatal diagnosis of cls.

  结论本研究是国内首次在分子水平确诊cls患者，为cls的基因诊断和产前诊断提供遗传基础。

• a 29 year old woman with a family history of hemophilia b asked for prenatal diagnosis in the 8th week of pregnancy.

  一例有血友病b家族史的29岁孕妇，于妊娠8周时要求对胎儿进行诊断。