De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms - Concepedia

Concepedia

Publication | Open Access

De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms

DOI Full Paper Access

42

Citations

43

References

2019

Year

Sandra Jansen, Ilse van der Werf, A. Micheil Innes, Alexandra Afenjar, Pankaj B. Agrawal, Ilse J. Anderson, Paldeep S. Atwal, Ellen van Binsbergen, Marie-José van den Boogaard, Lucia Castiglia,

European Journal of Human Genetics

Neurodevelopmental DisordersMendelian DisorderGenetic DisorderGeneticsPsychiatric GeneticsFragile X SpectrumBehavioral ProblemsSyndromic FormNeuroscienceDisease Gene IdentificationMedicineSocial SciencesNeurogeneticsDevelopmental Delay

References

	Year	Citations

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