Found 6 matching trials
Study of a Candidate Gene Involved in Goldenhar Syndrome. N/A The aim of this study is to identify of the first gene involved in the Gold...
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Multiple Locations
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Validation of a Clinical Screening Grid for Syndromic Schizophrenia NA Background:
Nowadays, despite a large number of studies about schizophreni...
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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 NA Congenital malformations concern 3% of pregnancies; most of them can be see...
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Genetics of Congenital Heart Disease N/A Congenital heart disease (CHD) is the most common type of birth defect but ...
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Nationwide Children's Hospital
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Study of the Value of Trio Exome Sequencing in the Etiological Assessment of Specific Non-syndromic Language and Learning Disorders NA Specific language and learning disorders (SLLD) affect around 5-10% of scho...
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CHU Dijon Bourgogne
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Clinic, Pathologic and Genetic Characterization of Patients With Familial Carcinoid Tumors (Study From the GTE, Groupe d'étude Des Tumeurs Endocrines) NA Small intestine carcinoid tumors are rare. Small intestine Familial Carcino...
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