• Fund Raising and/or Fund Distribution

• 64.

Renu Syndrome United

ReNU Syndrome Variants in RNU42 Uncovered as One of the Most Prevalent Causes of Neurodevelopmental Disorders Discovery Renews Hope for Affected Families Worldwide Characteristics may include Developmental Motor and Intellectual Delays Absent or Delayed Speech and Language Seizures Brain Abnormalities Small Head Size Distinct Facial Features Low Muscle Tone and Drooling Autism Spectrum Disorder Short Stature BoneSkeletal Anomalies Vision Issues and more More Information Big thanks to the researchers clinicians geneticists in these articlesfor this longawaited revelation.

Chromosome 22 Central Inc

🧬C22C official. Support & info for chromosome 22 disorders.

The Global Foundation for Peroxisomal Disorders

The GFPD's mission is to improve the lives of individuals with peroxisomal disorders by funding research, championing scientific collaboration, and empowering families and professionals through educational programs and support services.

• Research Institutes and/or Public Policy Analysis

• 67.

Forgotten Diseases Research Foundation

THE FORGOTTEN DISEASES RESEARCH FOUNDATION IS A NONPROFIT DEDICATED TO VERY RARE DISORDERS.

• Birth Defects, Genetic Diseases

• 68.

International Rett Syndrome Association, Inc.

We are transforming lives every day in our fight to treat and cure Rett syndrome and better the lives of families living with this devastating disorder.

• Diseases, Disorders, Medical Disciplines N.E.C.

• 69.

Trisomy 18 Bridge of Hope Foundation Inc

Search this site Building a Better Today and Tomorrow for Children with Trisomy 18 Hope Help and Information to help you advocate for your child I want you to know that you and your child are so very special.

• Birth Defects, Genetic Diseases Research

• 70.

Warner House Inc

See Sch O F. Jack Warner MD 19282004 a pediatrician dedicated to help patients achieve their highest potential.

• Birth Defects, Genetic Diseases

• 71.

LEO'S LIGHTHOUSE FOUNDATION INC

Leo’s Lighthouse is a non-profit making a difference in the lives of children affected by Bainbridge-Ropers Syndrome.

• Birth Defects, Genetic Diseases Research

• 72.

THE 11Q RESEARCH AND RESOURCE GROUP INC

home lifesaving protocols who we are frequently asked questions medical support donate More 11qRESEARCH RESOURCE GROUP WELCOMES YOU WHO WE ARE The mission of this website is to provide support and organizational efforts for the parents as well as friends and family of all children with 11th chromosome abnormalities including deletions monosomy duplications trisomy and translocations.