Prenatal sonographic phenotype of Raine syndrome: detection of novel <scp><i>FAM20C</i></scp> gene mutation at 20 weeks-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Prenatal sonographic phenotype of Raine syndrome: detection of novel FAM20C gene mutation at 20 weeks

Published:2023-07-05 Issue:2 Volume:62 Page:300-302
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound in Obstet & Gyne

Author:

Andrews A.¹,Nair S. B.²,Singh D.³^ORCID

Affiliation:

1. Department of Fetal Medicine Lifeline Super Speciality Hospital Adoor Kerala India

2. Department of Medical Genetics Lifeline Super Speciality Hospital Adoor Kerala India

3. Department of Radio‐diagnosis Prime Imaging and Prenatal Diagnostics Sector 24 D, Chandigarh India

Publisher

Wiley

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/uog.26200

Reference7 articles.

1. Raine syndrome: A rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findings

2. Raine syndrome: Prenatal diagnosis based on recognizable fetal facial features and characteristic intracranial calcification

3. Fetal ultrasonographic findings including cerebral hyperechogenicity in a patient with non-lethal form of Raine syndrome

4. Raine syndrome: Report of a novel mutation and review of the different antenatal imaging modalities used to diagnose this disease

5. Raine syndrome: An overview

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP