Concepedia

Publication | Open Access

Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation

DOIFull Paper Access

104

Citations

30

References

2016

Year

Karim Kouz, Stephanie Spranger, Diana Mitter, Vanesa López‐González, Sabine Lüttgen, Florian von Deimling, Christina Evers, Andreas Hahn, Maja Hempel, Ulrike Issa,
Genetics in Medicine

References

YearCitations

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