Found: 3
Select item for more details and to access through your institution.
A Novel Missense Mutation in TWNK Gene Causing Perrault Syndrome Type 5 in a Chinese Family and Review of the Literature.
- Published in:
- Pharmacogenomics & Personalized Medicine, 2022, v. 15, p. 1, doi. 10.2147/PGPM.S341172
- By:
- Publication type:
- Article
Oestradiol promotes the intrahepatic bile duct development of C57BL/6CrSlc mice during embryonic period via Notch signalling pathway.
- Published in:
- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 19, p. 9447, doi. 10.1111/jcmm.16888
- By:
- Publication type:
- Article
Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader–Willi syndrome.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 5, p. 438, doi. 10.1007/s12519-022-00653-y
- By:
- Publication type:
- Article