A unique case of recurrent fetal cystic hygroma: first fetus with an inherited heteromorphism of chromosome 1 (1qh+) and the second fetus with 69XXX triploidy-Reference-Cited by-同舟云学术

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A unique case of recurrent fetal cystic hygroma: first fetus with an inherited heteromorphism of chromosome 1 (1qh+) and the second fetus with 69XXX triploidy

Published:2021-04-01 Issue:3 Volume:61 Page:935-940
ISSN:1220-0522
Container-title:Romanian Journal of Morphology and Embryology
language:
Short-container-title:Rom J Morphol Embryol

Author:

Tica Oana Sorina, ,Gug Cristina,Tica Andrei Adrian,Busuioc Cristina Jana,Amiri Shahram,Tica Irina,Bică Brăiloiu George,Tica Vlad Iustin, , , , , , , ,

Publisher

Societatea Romana de Morfologie

Subject

Cell Biology,Developmental Biology,Embryology,General Medicine,Pathology and Forensic Medicine

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Approach and Management of Pregnancies with Risk Identified by Non-Invasive Prenatal Testing;Journal of Personalized Medicine;2024-03-29

2. Outcome of Sclerotherapy in a Preterm Infant with a Giant Fetal Neck Lymphatic Malformation: A Case Report;International Journal of Women's Health;2023-11

3. Recurrent Cystic Hygroma and Poor Pregnancy Outcomes in a Single Patient.;2023-10-12

4. Current Perspectives of Prenatal Cell-free DNA Screening in Clinical Management of First-Trimester Septated Cystic Hygroma;International Journal of Women's Health;2022-10

5. The Effect of Prenatal Ultrasound Score on the Evaluation of Cesarean Section with Placenta Previa and the Prognosis of Mother and Child;Advances in Clinical Medicine;2022

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