Prenatal ultrasound-assisted identification of multiple malformations caused by a deletion in the long-arm end of chromosome 7 and review of the literature-Reference-Cited by-同舟云学术

Prenatal ultrasound-assisted identification of multiple malformations caused by a deletion in the long-arm end of chromosome 7 and review of the literature

Published:2020-11-19 Issue: Volume: Page:1-5
ISSN:1476-7058
Container-title:The Journal of Maternal-Fetal & Neonatal Medicine
language:en
Short-container-title:The Journal of Maternal-Fetal & Neonatal Medicine

Author:

Zhao Xuliang¹,Sun Weiwei²,Jia Jian-an¹,Wei Zhuojun³,Li Xu⁴,Liao Wenbin⁵,Wu Juanshu¹,Wang Yajian²,Tian Ruixia³

Affiliation:

1. Department of Clinical Laboratory, The No. 901 Hospital of the Joint Service of the People’s Liberation Army, Hefei, P.R. China;

2. Beijing Chigene Translational Medicine Research Center, Beijing, P. R. China;

3. Department of Obstetrics and Gynecology, The No. 901 Hospital of the Joint Service of the People’s Liberation Army, Hefei, P. R. China;

4. Department of Radiology, Anhui Provincial Children’s Hospital, Hefei, P. R. China;

5. Department of Radiology, The No. 901 Hospital of the Joint Service of the People’s Liberation Army, Hefei, P. R. China

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/14767058.2020.1849104

Reference19 articles.

1. Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations

2. Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations

3. Hedgehog Signal and Genetic Disorders

4. Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly

5. MiR-130a-5p/Foxa2 axis modulates fetal lung development in congenital diaphragmatic hernia by activating the Shh/Gli1 signaling pathway

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