30.05.2019 · Gabriele-de Vries syndrome is characterized by mild-to-profound developmental delay / intellectual disability (DD/ID) in all affected ...
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What is Gabriele-de Vries syndrome?
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المساهمون: CHU Clermont-Ferrand, University of Western Ontario (UWO), London Health Sciences Center (LHSC), CHU Montpellier, Centre Hospitalier Régional ...
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30.05.2019 · Clinical characteristics: Gabriele-de Vries syndrome is characterized by mild-to-profound developmental delay / intellectual disability (DD/ID) ...
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Gabriele-de Vries syndrome is a rare autosomal dominant genetic disease caused by de novo pathogenic variants in the Yin Yang 1 (YY1) gene.
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CLINICAL CHARACTERISTICS:Gabriele-de Vries syndrome is characterized by mild-to-profound developmental delay / intellectual disability (DD/ID) in all ...
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Disease code: OMIM:617557 · Associated therapeutic area(s):. Abnormality of the musculoskeletal system (HP:0033127) · Prenalytics: 5 mL whole blood or DNA sample
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... Gabriele-de Vries syndrome. Test guide ... Gabriele-de Vries syndrome. International Division. Monday-Friday : 8.30 am - 6.30 pm (GMT + 1) T. : +33 4 72 80 23 85
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Each time a person has a genetic test, their genetic test result will be documented in a genetic report. A genetic report is a formal document from a ...
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