Found: 5
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Mutational analysis of ATP7B in north Chinese patients with Wilson disease.
- Published in:
- Journal of Human Genetics, 2013, v. 58, n. 2, p. 67, doi. 10.1038/jhg.2012.134
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- Article
Application of a low copper diet guidance based on food exchange portions in children with hepatolenticular degeneration.
- Published in:
- Chinese Journal of Contemporary Pediatrics, 2023, v. 25, n. 6, p. 612, doi. 10.7499/j.issn.1008-8830.2212034
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- Article
Adenovirus-mediated Interferon-γ Gene Therapy Induced Human Pancreatic Carcinoma Capan-2 Cell Apoptosis In Vitro and In Vivo.
- Published in:
- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2013, v. 296, n. 4, p. 604, doi. 10.1002/ar.22661
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- Article
Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype–phenotype analysis of 105 patients.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 7, p. 674, doi. 10.1007/s12519-022-00674-7
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- 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
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- Article