File:Axillary freckling in neurofibromatosis type 1.png

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Axillary freckling in neurofibromatosis type 1

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Description
English: Axillary freckling in neurofibromatosis type 1
Date
Source Serra G, Antona V, Corsello G, Zara F, Piro E, Falsaperla R (2019). "NF1 microdeletion syndrome: case report of two new patients.". Ital J Pediatr 45 (1): 138. DOI:10.1186/s13052-019-0718-7. PMID 31703719. PMC: 6839219. (Creative Commons Attribution 4.0 International license.)
Author Serra G, Antona V, Corsello G, Zara F, Piro E, Falsaperla R

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Date/TimeThumbnailDimensionsUserComment
current12:28, 5 June 2023Thumbnail for version as of 12:28, 5 June 2023896 × 1,336 (1.16 MB)Mikael Häggström (talk | contribs)Uploaded a work by Serra G, Antona V, Corsello G, Zara F, Piro E, Falsaperla R from {{cite journal| author=Serra G, Antona V, Corsello G, Zara F, Piro E, Falsaperla R| title=NF1 microdeletion syndrome: case report of two new patients. | journal=Ital J Pediatr | year= 2019 | volume= 45 | issue= 1 | pages= 138 | pmid=31703719 | doi=10.1186/s13052-019-0718-7 | pmc=6839219 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=...

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