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pro vyhledávání: '"Samantha Vershaw"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 6, Pp n/a-n/a (2024)
Abstract Background Patients with uncommon genetic conditions often face limited in‐person resources for social and informational support. Hypermobile Ehlers–Danlos syndrome (hEDS) is a rare or underdiagnosed hereditary disorder of the connective
Externí odkaz:
https://doaj.org/article/0af1686f0ede42d8a17e8ce2bacd7509
