First trimester diagnosis of 22q11.2 microdeletion-syndrome associated with increased fetal nuchal t

来源 :第十四次全国医学遗传学学术会议 | 被引量 : 0次 | 上传用户：TSNT1234

【摘要】

：

　　OBJECTIVE: To present chromosomal microarray analysis (CMA) characterization of 22q11.2 microdeletion presenting with increased nuchal translucency (NT) and

【作者】

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CaoDing-ya;LiNan;ChenMin;

【机构】

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Center for Prenatal Diagnosis, The Third Affiliated Hospital of Guang Zhou Medical University, Key L

【出处】

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第十四次全国医学遗传学学术会议

【发表日期】

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2015年期

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　　OBJECTIVE: To present chromosomal microarray analysis (CMA) characterization of 22q11.2 microdeletion presenting with increased nuchal translucency (NT) and congenital heart defects.CASE REPORT: We report on a fetus presenting with increased nuchal translucency at 12+3 weeks' gestation.

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First trimester diagnosis of 22q11.2 microdeletion-syndrome associated with increased fetal nuchal t

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