30.05.2019 · Gabriele-de Vries syndrome is characterized by mild-to-profound developmental delay / intellectual disability (DD/ID) in all affected ...
Review Clinical analysis of Gabriele-de Vries caused by YY1 mutations and literature review. Yang J, Yu C, Lyn N, Liu L, Li D, Shang Q. Mol Genet Genomic Med.
Reader in Quantum Information, Queen's University Belfast - Cited by 6206 - Quantum Information - Ultracold atoms - Trapped ions - Condensed ...
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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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23.12.2020 · Gabriele-de Vries syndrome (GADEVS), also known as YY1 haploinsufficiency syndrome, is a very rare autosomal dominant neurodevelopmental ...
His work predominantly makes use of animal imagery to discuss contemporary concerns - both environmental and societal. Jacobs explores examples from nature ...
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Visit random profile Advanced search · 2024 IIHF ... Czechia Q. USA Jonny Rossmann (G) · USHS-MN. Austria ... Pieve Di Cadore U19 · Italy U19, Asst. Coach. Pieve Di ...
Search by expertise, name or affiliation. Gabriele De Chiara. View Scopus Profile. Gabriele De Chiara. Dr. Reader, School of Mathematics and Physics · Centre ...
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Prof. Dr. Gabriele Taentzer · Professor of Software Technology at the Faculty of Mathematics and Computer Science · Liaison lecturer at Association for Computer ...