Prenatal Diagnosis: 2582 Clinical Trials, Page 1 of 259

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Development of Non-Invasive Prenatal Diagnosis for Single Gene Disorders

Condition(s):Invasive PreNatal Diagnosis in a Context of Family History of Single-gene Disorders, Including; Sickle Cell Disease; Cystic Fibrosis; Fragile X Syndrome; Proximal Spinal Muscular Atrophy; Myotonic Dystrophy; Muscular Dystrophy, Duchenne; Muscular Dystrophy, Becker; Neurofibromatosis-Noonan Syndrome; Huntington Disease; Hemophilia A; Hemophilia B; MODY2 Diabetes; X-Linked Hydrocephalus; Autosomal Recessive Polycystic Kidney DiseaseLast Updated:February 28, 2024Not yet recruiting

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