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An Extremely Rare SRD5A2 Gene c.485A>C Mutation in a Compound Heterozygous Newborn with Disorders of Sex Development First Identified in Vietnam.
- Published in:
- 2022
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- Publication type:
- Case Study
An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32-11.22.
- Published in:
- Nagoya Journal of Medical Science, 2020, v. 82, n. 4, p. 783, doi. 10.18999/nagjms.82.4.783
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- Publication type:
- Article
Helicobacter pylori 23S rRNA gene mutations associated with clarithromycin resistance in chronic gastritis in Vietnam.
- Published in:
- Journal of Infection in Developing Countries, 2018, v. 12, n. 7, p. 526, doi. 10.3855/jidc.10000
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- Publication type:
- Article