Molecular and clinical characterization of new patient with 1,08 Mb deletion in 10p15.3 region.
- Published in:
- Molecular Cytogenetics (17558166), 2017, v. 10, n. 1, p. 1, doi. 10.1186/s13039-017-0336-2
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- Publication type:
- Article
Works matching IS 17558166 AND DT 2017 AND VI 10 AND IP 1
Results: 3
1
2
CMA analysis identifies homozygous deletion of MCPH1 in 2 brothers with primary Microcephaly-1.
- Published in:
- Molecular Cytogenetics (17558166), 2017, v. 10, n. 1, p. 1, doi. 10.1186/s13039-017-0334-4
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- Publication type:
- Article
3
A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case report.
- Published in:
- 2017
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- Publication type:
- Case Study