De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome - Concepedia

Concepedia

Publication | Open Access

De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome

DOI Full Paper Access

19

Citations

21

References

2020

Year

Roser Ufartes, Hanna Berger, Katharina Till, Gabriela Salinas, Marc Sturm, Janine Altmüller, Peter Nürnberg, Hölger Thiele, Rudolf Funke, N. Apeshiotis,

References

	Year	Citations

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