Associated Papers
Germline mutations and developmental mosaicism underlying EGFR-mutant lung cancer.
Burr R et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
37808694 (PubMed )
Supplement: media-2.xlsx › Patient_6
A new variant of MYCN gene as a cause of Feingold syndrome.
Zeka N et al.
Clinical Case Reports, 2022
Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.
Cognet M et al.
European Journal of Human Genetics : Ejhg, 2011
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