Browse Studies — Arctuva

Genetic Modifiers of 22q11.2 Deletion Syndrome

22q11.2 deletion syndrome is a genetic disorder that can cause heart defects, facial abnormalities, and developmental and learning disabilities. The severity o…

DiGeorge Syndrome22q11.2 Deletion Syndrome

Estimated

~$10 – $750

Albert Einstein College of MedicineNCT00556530

ADVANCE Study: Assay Development and Validation for Pre-Natal and Obstetric Conditions

The goal of the ADVANCE (Assay Development and Validation for Pre-Natal and Obstetric Conditions) study is to compare the concordance of results of a novel non…

Pregnant IndividualsAneuploidyDown Syndrome (Trisomy 21)+4 more

Estimated

~$10 – $1,050

BillionToOne Inc.NCT07643896

Functional and Neurodevelopmental Outcomes Following Intensive Multimodal Neurorehabilitation in Pediatric Patients With Neurodevelopmental Disorders, Including Chromosomal Abnormalities

This observational study evaluates functional and developmental outcomes in pediatric participants undergoing a two week intensive multimodal neurorehabilitati…

Neurodevelopmental DisordersNeurodevelopmental Disorders (NDD)Neurodevelopmental Disorders and Developmental Abnormalities+20 more

Estimated

~$10 – $1,125