Phelan McDermid Syndrome Foundation

Official site of the Phelan-McDermid Syndrome Foundation.

• Remedial Reading, Reading Encouragement

• 20.

Firefly Fund

A nonprofit that provides crucial support for research and education necessary to accelerate cures for rare genetic diseases that affect children.

• Fund Raising and/or Fund Distribution

• 21.

Eleanor Kaplan Foundation Inc

To raise funds and awareness to develop cures for Ultra Rare Neurodegenerative Diseases.

Beck Fahrner Syndrome Foundation

Our mission is to accelerate full spectrum research to cure Beck-Fahrner Syndrome (TET3 deficiency) and to empower affected families with information, knowledge, and connectivity.

Hunters CMT4B3 Research Foundation Inc

Pioneering cutting edge scientific research to develop treatments for CMT4B3 patients and children with rare neuromuscular diseases.

• Specifically Named Diseases

• 24.

Andrews Firefly Fund

A nonprofit that provides crucial support for research and education necessary to accelerate cures for rare genetic diseases that affect children.

• Birth Defects, Genetic Diseases

• 25.

Mitchell and Friends Foundation

To raise awareness of Mitchell Syndrome and support research into possible treatments and cures Raising awareness of Mitchell Syndrome and supporting families and children with this rare neurological disease.

• Specifically Named Diseases Research

• 26.

THE FOCUS FOUNDATION INC

OUR FOCUS:Helping children who have* X & Y Variations* Dyslexia * DyspraxiaEarly Identification + Tar Early Awareness Detection Treatment for X Y Chromosomal Variation Disorders X Y Chromosomal Disorders 47 XXY 47 XYY 47 XXX Learn more about them.

• Birth Defects, Genetic Diseases Research

• 27.

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.