Cite
HARVARD Citation
Cavaliere, E. et al. (2021). NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome. Clinical genetics. 100 (1), pp. 114-116. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Cavaliere, E. et al. (2021). NKX2.1 run‐on mutation associated to familial brain–lung–thyroid syndrome. Clinical genetics. 100 (1), pp. 114-116. [Online].