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What is Gabriele de Vries syndrome symptoms?
What is Jansen de Vries syndrome?
13.03.2023 · Gabriele-de Vries syndrome is a rare autosomal dominant genetic disease caused by de novo pathogenic variants in the Yin Yang 1 (YY1) gene.
Gabriele-de Vries syndrome is a rare autosomal dominant genetic disease caused by de novo pathogenic variants in the Yin Yang 1 (YY1) gene.
Es fehlt: researchgate. 369580033_First_Reported_Case_of_Gabriele-
30.05.2019 · PDF | Clinical characteristics Gabriele-de Vries syndrome is characterized by mild-to-profound developmental delay / intellectual disability ...
Es fehlt: 369580033_First_Reported_Case_of_Gabriele- de_Vries_Syndrome_with_Spinal_Dysraphism
02.01.2024 · Herein, we report a case involving a rare early childhood epilepsy phenotype in a patient diagnosed with GADEVS based on the typical clinical ...
Es fehlt: q= https:// 369580033_First_Reported_Case_of_Gabriele-
30.05.2019 · Gabriele-de Vries syndrome is characterized by mild-to-profound developmental delay / intellectual disability (DD/ID) in all affected ...
Es fehlt: researchgate. 369580033_First_Reported_Case_of_Gabriele- de_Vries_Syndrome_with_Spinal_Dysraphism