Wangler Lab Logo
  • Home
  • Research
    • Lab Research
      • Gene Discovery in Mendelian Disorders
      • Model Organisms of Mendelian Disorders
      • Peroxisome and Organelle Dynamics
    • Clinical Research
      • Correlates of Peroxisomal Disorders
      • Mendelian Disease Gene Discovery
      • Undiagnosed Diseases Network
  • People
    • Meet Our Group
    • The SFARI Team
    • The UDN Team
    • Medical Students
  • Positions
  • Publications
  • Resources
    • Resources
    • MARRVEL
    • For Rotation Students
  • Contact Us
    • In the News

Resources

Posted on January 21, 2016July 16, 2016 by mfwangler
Centers for Mendelian Genomics

Centers for Mendelian Genomics

Undiagnosed Diseases Network

Undiagnosed Diseases Network

https://sfari.org

https://sfari.org

SFARI Gene

SFARI Gene

Drosophila Gene Disruption Project

Drosophila Gene Disruption Project

GFPD

GFPD

Neurological Research Institute

Neurological Research Institute

Deciphering the Mechanisms of Developmental Disorders

Deciphering the Mechanisms of Developmental Disorders

PeroxisomeDB

PeroxisomeDB

IMPC

IMPC

Lichtarge Lab

Evolutionary Action from Lichtarge Lab

Tweets by mfwangler
Tweets by @mfwangler

In the News

$75,000 Research Grant Awarded in Effort to Accelerate Treatment Options for Rare Diseases

Mystery Condition Gives Way to Bright Future for 10-Year-Old

These Houston Doctors Seek to Diagnose the Previously Un-Diagnosable

Michael Wangler Co-Authors a Chapter in a New Book with Hugo Bellen Designed for Encouraging Clinical Researchers and Detailing Basic Methods in Drosophila Research

Reagan’s Story

More News Articles...

Recent Posts

  • On Rare Disease Day, Remember What Family Organizations Can Do February 27, 2018
  • THE TOP TEN RARE DISEASE PAPERS OF ALL TIME February 27, 2017
  • Why Drosophila? Learning to Fly in the UDN January 6, 2017
A SiteOrigin Theme