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Apparently Balanced Chromosomal Translocation/ Next-generation Sequencing/ Intellectual Disability
Condition(s):Intellectual Disability; Congenital AbnormalitiesLast Updated:March 23, 2017Completed
Gene Abnormality: 999 Clinical Trials, Page 5 of 100
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Study of the Involvement of 15q11 – q13 Chromosome Region and CYFIP1 Gene in Autism. Attempt a Genotype-phenotype Correlation
Condition(s):Autistic DisorderLast Updated:August 11, 2016Completed
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Realization of Sequencing of All Known Human Genes in Case of Detection of Cerebral, Renal or Ophthalmological Fetal Malformations During Pregnancy in Order to Make an Etiological Diagnosis and to Precise the Fetal Prognosis
Condition(s):Fetal Malformation; Pregnancy Related; Rare Genetic DiseaseLast Updated:November 13, 2020Recruiting
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Network Of Clinical Research Studies On Craniosynostosis, Skull Malformations With Premature Fusion Of Skull Bones
Condition(s):CraniosynostosisLast Updated:July 7, 2022Recruiting
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Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associated Anomalies
Condition(s):Congenital Fibrosis of Extraocular Muscles; Duane Retraction Syndrome; Duane Radial Ray Syndrome; Mobius Syndrome; Brown Syndrome; Marcus Gunn Syndrome; Strabismus Congenital; Horizontal Gaze Palsy; Horizontal Gaze Palsy With Progressive Scoliosis; Facial Palsy; Facial Paresis, Hereditary, Congenital; Third Nerve Palsy; Fourth Nerve Palsy; Sixth Nerve Palsy; Synkinesis; Ocular Motility Disorders; Levator-Medial Rectus Synkinesis; Athabaskan Brainstem Dysgenesis; Tongue Paralysis; Ninth Nerve Disorder; Fifth Nerve Palsy; Seventh Nerve Palsy; Eleventh Nerve Disorder; Twelfth Nerve Disorder; Vagus Nerve Paralysis; Moebius SequenceLast Updated:September 10, 2021Recruiting
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Vascular Malformations and Abnormalities of Growth
Condition(s):AbnormalityLast Updated:January 7, 2014Completed
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Study of Muscle Abnormalities in Patients With Specific Genetic Mutations
Condition(s):Cardiomyopathy, Hypertrophic; Muscular Dystrophy, OculopharyngealLast Updated:March 4, 2008Completed
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PCM1-JAK2 in Therapy Related Neoplasms
Condition(s):Detection of PCM1-JAK2 Fusion Gene by FISH in the Two Types of t-MDS/AML and Relationship Between PCM1-JAK2 Fusion Gene and Cumulative Dose, Dose IntensityLast Updated:May 9, 2019Unknown status
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Genetic and Nutritional Causes of Heart Birth Defects
Condition(s):Heart Defects, CongenitalLast Updated:July 29, 2016Completed
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Seronegatives and Metabolic Abnormalities Protocol 2 (SAMA002): Study to Compare the Effect of Kaletra and Combivir® in HIV-Negative Healthy Subjects
Condition(s):HIV Infections; Dyslipidemias; Glucose Metabolism Disorders; Metabolic Diseases; Lipodystrophy; Cardiovascular DiseaseLast Updated:April 12, 2012Completed