Concepedia

Publication | Open Access

An example of the utility of genomic analysis for fast and accurate clinical diagnosis of complex rare phenotypes

DOIFull Paper Access

16

Citations

11

References

2017

Year

Polona Le Quesne Stabej, Chela James, Louise Ocaka, Mehmet Tekman, Stephanie Grünewald, Emma Clement, Horia Stanescu, Robert Kleta, Deborah Morrogh, Alistair Calder,
Orphanet Journal of Rare Diseases

References

YearCitations

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