Fetal presentation of chondrodysplasia with joint dislocations, GPAPP type, caused by novel biallelic IMPAD1 variants

Author:

Venkatapuram Vijaya Sree12,Aggarwal Shagun12ORCID,Kulkarni Aditya Deepak3,Vineeth Venugopal Satidevi2,Bhikaji Dalal Ashwin2ORCID,Bhat Venkatraman4,Kiran Lavanya5,Patil Siddaramappa Jagdish6ORCID

Affiliation:

1. Department of Medical Genetics Nizam's Institute of Medical Sciences Hyderabad India

2. Division of Diagnostics Centre for DNA Fingerprinting & Diagnostics Hyderabad India

3. Department of Pathology Apollo Hospitals Hyderabad India

4. Department of Radiology, Mazumdar Shaw Medical Center Narayana Hrudayalaya Hospitals Bangalore India

5. Department of Obstetrics and Gynecology, Mazumdar Shaw Medical Center Narayana Hrudayalaya Hospitals Bangalore India

6. Division of Medical Genetics, Mazumdar Shaw Medical Center Narayana Hrudayalaya Hospitals Bangalore India

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3