Overview
Xiongwei Fan practices practicing medicine in Changsha, China.
Their clinical expertise encompasses Chromosome 18p Deletion, Achondrogenesis, VACTERL Association, and Acromesomelic Dysplasia Campailla Martinelli Type.
They are actively involved in clinical research, co-authoring 34 peer reviewed articles.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Frequently Asked Questions about Xiongwei G. Fan
Is Xiongwei G. Fan a top-rated expert for Chromosome 18p Deletion?
MediFind is an objective health platform that identifies experts based on real-world data. Xiongwei G. Fan is classified as an Experienced expert for Chromosome 18p Deletion, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Xiongwei G. Fan participate in research or clinical trials?
Yes. Xiongwei G. Fan has published 34 articles and abstracts on conditions like Chromosome 18p Deletion. You can view a list of Xiongwei G. Fan's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Experienced
- AchondrogenesisFan isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaFan isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Brachydactyly Mononen Type
- ChondrodystrophyFan isExperienced. Learn about Chondrodystrophy.
- Chromosome 18p DeletionFan isExperienced. Learn about Chromosome 18p Deletion.
- HoloprosencephalyFan isExperienced. Learn about Holoprosencephaly.
- Patent Foramen OvaleFan isExperienced. Learn about Patent Foramen Ovale.
- Schwartz-Jampel SyndromeFan isExperienced. Learn about Schwartz-Jampel Syndrome.
- Tetralogy of FallotFan isExperienced. Learn about Tetralogy of Fallot.
- VACTERL AssociationFan isExperienced. Learn about VACTERL Association.
- X-Linked Spondyloepiphyseal Dysplasia Tarda