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A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case report

机译：在胎儿中观察到胎儿的一种罕见的心脏表型，胎儿，具有1p36缺失综合征和平衡易位：产前案例报告

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Li Gao; Junyu Zhang; Xu Han; Wenjing Hu; Jinling Sun; Yuru Tan; Xinrong Zhao; Renyi Hua; Shan Wang; Yan Zhang; Yanlin Wang; Yi Wu;
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1. Prenatal diagnosis of a fetus with terminal deletion of chromosome 1 (q43) in first-trimester screening: is there a characteristic antenatal 1q deletion phenotype? A case report and review of the literature. [J] . Wagner N, Guengoer E, Mau Holzmann UA, Fetal diagnosis and therapy . 2011,第3期

机译：在孕早期筛查中发现胎儿在染色体1末端末端缺失（q43）的产前诊断：是否存在特征性的产前1q缺失表型？病例报告和文献复习。
2. Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature. [J] . Faivre L, Morichon Delvallez-N, Viot G, Prenatal Diagnosis . 1999,第1期

机译：胎儿多种畸形的产前检测1p36缺失和文献复习。
3. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother [J] . Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Taiwanese journal of obstetrics and gynecology . 2021,第1期

机译：家族22Q11.2妊娠期缺失综合征的产前诊断胎儿和母亲伴随的心脏和泌尿道异常
4. Prenatal observation of heart rate sequences presenting entropic analogies with Sudden Infant Death Syndrome: Preliminary report [C] . Zemb Patrick, Goncalves Hernani, Bellec Jean-Yves, IEEE International symposium on computer-based medical systems . 2013

机译：呈现熵类似婴儿猝死综合征的心率序列的产前观察：初步报告
5. Information and Resources Provided to Patients Receiving a Prenatal Diagnosis of Down Syndrome as Reported by Health Care Professionals [D] . King, Annette Marie 2012

机译：根据卫生保健专业人员的报告，向患有唐氏综合症产前诊断的患者提供的信息和资源
6. A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case report [O] . Li Gao, Junyu Zhang, Xu Han, 2020

机译：在胎儿中观察到胎儿的一种罕见的心脏表型胎儿具有1p36缺失综合征和平衡易位：产前案例报告
7. Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings [O] . Chih-Ping Chen, Ming Chen, Yi-Ning Su, 2010

机译：染色体1p36缺失综合征：产前诊断，分子细胞遗传学表征和胎儿超声检查结果

A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case report

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