Replacement of Cytogenetics by aCGH in Prenatal Diagnosis
Condition(s):Prenatal DiagnosisLast Updated:May 20, 2019Completed
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Condition(s):Prenatal DiagnosisLast Updated:May 20, 2019Completed
Condition(s):Cystic FibrosisLast Updated:January 27, 2020Unknown status
Condition(s):Prenatal Diagnosis and Closed-loop Management System of Congenital Talipes EquinovarusLast Updated:December 6, 2022Recruiting
Condition(s):Trisomy 21Last Updated:July 7, 2021Unknown status
Condition(s):Non Invasive Prenatal DiagnosisLast Updated:December 30, 2020Completed
Condition(s):Noninvasive Mucinous Cystadenocarcinoma of OvaryLast Updated:December 31, 2014Unknown status
Condition(s):Comparative Genomic HybridizationLast Updated:April 6, 2021Unknown status
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
Condition(s):Prenatal; Genome-wide High Throughput SequencingLast Updated:June 22, 2022Recruiting
Condition(s):Copy Number Variation; GenomeLast Updated:September 23, 2020Unknown status
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