• Birth Defects, Genetic Diseases Research

• 190.

Center for Human Genetics Inc

TO FUNCTION AS A LOCAL AND NATIONAL CLINIC AND DIAGNOSTIC REFERENCE RESOURCE FOR BIRTH DEFECT AND GENETIC DISORDERS; TO PROVIDE TECHNOLOGY AND SERVICES TO REFERRING PHYSICIANS AND PATIENTS FOR THE BENEFIT OF ALL PERSONS SUFFERING FROM ILLNESS, DEFECTS OR DISORDERS; TO TEACH MEDICAL STUDENTS, RESIDENTS, FELLOWS AND OTHER PERSONNEL ENGAGED IN HEALTH SERVICES AND HEALTH EDUCATION; TO ADVANCE SCIENTIFIC KNOWLEDGE THROUGH RESEARCH; TO TAKE ACTIVE PART IN THE PLANNING FOR AND THE PROMOTION OF THE SPECIFIC GENETIC AND GENERAL MENTAL AND PHYSICAL HEALTH AND HUMAN NEEDS AND INTERESTS OF THE LOCAL AND NATIONAL PATIENT POPUATION AND THEIR PHYSICIANS; TO PROVIDE SERVICES RELATED TO GENETICS; TO GATHER DATA AND ANALYZE IT FOR THE PURPOSE OF SHARING IT GENERALLY WITH THE LOCAL, NATIONAL AND INTERNATIONAL MEDICAL COMMUNITIES; TO IMPROVE AND DEVELOP TESTING PROTOCOLS AND KNOWLEDGE AND TO SHARE SUCH RESULTS FREELY AND OPENLY; TO ESTABLISH, OWN, OPERATE, CONDUCT OR MAINTAIN FACILITIES FOR TEACHING.

• Birth Defects, Genetic Diseases

• 191.

Nergg Inc

Raise awareness and educate regarding the effects of genetics on health 1977 2025Celebrating 48 Yearsof Education Collaboration and more.

• Biomedicine, Bioengineering

• 192.

Biopharmaceutical Technology Center Institute Inc

Welcome to the BTC Institute PHOTO Dane County Biotechnology Youth Apprenticeship Program 2024 Yearend Celebration at the Kornberg Center Promega Corporation Join us for the Wisconsin Stem Cell Symposium on April 2nd 2025Registration is now open.

• Public Foundations

• 193.

James G Delmauro Foundation Inc

The Michael J. Fox Foundation is dedicated to finding better treatments and, ultimately, a cure for Parkinson’s disease.

Rheumatology Research Foundation

Advancing research and training to improve the health of people with rheumatic diseases.

Decoding Developmental Epilepsies

We serve two distinct communities. First, we serve those living with SCN8A and their families.

Foxg1 Research Foundation

FOXG1 syndrome is a childhood neurological genetic disorder and is a key to understanding many brain disorders.

• Biological, Life Science Research (includes Marine Biology, Physiology, Biochemistry, Genetics, Biotechnology, etc.)

• 197.

KEYSTONE SYMPOSIA ON MOLECULAR

A catalyst for accelerating life science discovery and connecting scientists within and across disciplines at symposia worldwide.

THE CANCER LEAGUE INC

Seed the cure. Fund the dreams that lead to breakthroughs.