
Curren’s Journey: Only the Fourth Person in the World to Be Diagnosed with HIVEP2 Syndrome
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DDX3X: When Whole Exome Sequencing Reveals a Gene Variant that Science Hasn’t Caught Up To
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Mom Spreads Awareness About Rare SYNGAP-1 Gene Disorder After Son’s Diagnosis
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Global Genes Partners With SWAN USA To Help Undiagnosed Rare Disease Patients Seek A Medical Diagnosis Through Free Whole Exome Sequencing Program
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