Anne Marie Jelsig
0000-0002-0916-4517
Rigshospitalet
4 papers found
Refreshing results…
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology
The Management of Peutz–Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline
Two cases of somatic STK11 mosaicism in Danish patients with Peutz–Jeghers syndrome
A case of microdeletion of 19p13 with intellectual disability, hypertrichosis, synophrys, and protruding front teeth
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