Prenatal diagnosis of fetuses with Emanuel syndrome: Results of ultrasound examination and invasive genetic testing.
第一作者:
Xiulan,Hao
第一单位:
Department of Obstetrics and Gynecology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
作者:
主题词
染色体障碍(Chromosome Disorders);腭裂(Cleft Palate);女(雌)性(Female);胎儿(Fetus);基因检测(Genetic Testing);心脏缺损, 先天性(Heart Defects, Congenital);人类(Humans);肌张力过低(Muscle Hypotonia);颈部透明带检查(Nuchal Translucency Measurement);妊娠(Pregnancy);产前诊断(Prenatal Diagnosis);回顾性研究(Retrospective Studies);易位, 遗传(Translocation, Genetic);超声检查, 产前(Ultrasonography, Prenatal)
DOI
10.1002/pd.6098
PMID
35043432
发布时间
2022-05-11
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Prenatal diagnosis
469-477页
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