Birth Defects, Genetic Diseases Research
List of non-profit organizations working on Birth Defects, Genetic Diseases Research .
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Birth Defects, Genetic Diseases Research
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55.
Team Grayson Inc
Team Grayson is a non-profit dedicated to ending Necrotizing Enterocolitis (NEC) through education, raising awareness and funding NEC research.
1280
WEST NEWBURY
MASONIC MEDICAL RESEARCH LABORATORY
Masonic Medical Research Institute (MMRI) is a leading non-profit center for science research and innovation.
1249
Utica
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Fund Raising and/or Fund Distribution
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57.
Ellie White Foundation for Rare Genetic Disorders Inc
We will not give up until a cure for Wolfram syndrome is found for Ellie and the children suffering from this disorder.
1161
Centennial
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Birth Defects, Genetic Diseases Research
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58.
Greenwood Genetic Center Inc
Clinical geneticists, laboratory diagnosticians, researchers, and educators with a passion for patient care.
1144
Greenwood
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Birth Defects, Genetic Diseases Research
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59.
CHILDRENS FUND FOR GLYCOGEN STORAGE DISEASE RESEARCH
The Children's Fund for GSD Research is dedicated to finding a cure for Glycogen Storage Disease 1a: a 501(c)(3) run by parents and family of patients.
1068
Cheshire
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Birth Defects, Genetic Diseases Research
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60.
Study the Options Please Inc
Care Net Pregnancy Center of Wayne County provides support, education, and hope to women facing unplanned pregnancies.
1000
Newark
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Birth Defects, Genetic Diseases Research
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61.
International Mammalian Genome Society Inc
The International Mammalian Genome Society fosters research in mammalian genetics, from sequencing and functional genomics to mutagenesis and mutant analysis.
976
Oak Ridge
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Birth Defects, Genetic Diseases Research
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62.
Canavan Research Foundation, Inc.
Our mission is to fund and support research to cure Canavan Disease and apply these findings to create therapies for other genetic brain diseases.
891
New Fairfield
Ring14 USA Outreach Inc
Ring14 Syndrome, Rare disease, Rare epilepsy, nonprofit, support, advocacy, research Ring14 USA is nonprofit 501(c)(3) that supports children and families affected by the rare syndromes of the 14th chromosome, such as Ring14 syndrome.
860
Ring14 USA