Works matching IS 17558166 AND DT 2025 AND VI 18 AND IP 1
Results: 5
Novel MSH6 exon 5–6 skipping variant in a Taiwanese family with Lynch syndrome: implications for genetic testing and cancer management.
- Published in:
- Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00708-5
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- Publication type:
- Article
Whole genome uniparental isodisomy detected using single nucleotide polymorphism (SNP) microarray in molar pregnancy: a case report.
- Published in:
- 2025
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- Publication type:
- Case Study
Prevalence of CNVs on the X chromosome in patients with neurodevelopmental disorders.
- Published in:
- Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00703-w
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- Article
Preparing high-quality chromosome spreads from Crocus species for karyotyping and FISH: High-quality chromosome spreads in Crocus: A. El-nagish et al.
- Published in:
- Molecular Cytogenetics (17558166), 2025, v. 18, n. 1, p. 1, doi. 10.1186/s13039-025-00706-7
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- Publication type:
- Article
Phenotypic and genotypic insights into concurrent tertiary trisomy for 9p and 18p.
- Published in:
- 2025
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- Publication type:
- Case Study