| DC Field | Value | Language |
|---|
| dc.contributor.author | Odalis Molina-Gamboa | - |
| dc.contributor.author | Andurina Barrios-Martinez | - |
| dc.contributor.author | Alina Garсia-Garсia | - |
| dc.contributor.author | Luanda Maceira | - |
| dc.contributor.author | Luis A. Mendez-Rosado | - |
| dc.date.accessioned | 2022-04-13T13:54:28Z | - |
| dc.date.available | 2022-04-13T13:54:28Z | - |
| dc.date.issued | 2021 | - |
| dc.identifier.citation | Essentially pure partial trisomy 6(p21.31-p25) (case report and literature review) / Odalis Molina-Gamboa [et al.] // Научные результаты биомедицинских исследований. - 2021. - Т.7, №4.- P. 322-329. - Doi: 10.18413/2658-6533-2021-7-4-0-1. - Refer.: p. 327-329. | ru |
| dc.identifier.uri | http://dspace.bsu.edu.ru/handle/123456789/46040 | - |
| dc.description.abstract | To achieve a better clinical delineation of the 6p syndrome through the description of a patient with partial trisomy 6(p21.31-p25) comparing his characteristics with international reports and to discuss aspects of the phenotype of this syndrome | ru |
| dc.language.iso | en | ru |
| dc.subject | medicine | ru |
| dc.subject | medical genetics | ru |
| dc.subject | trisomy 6p | ru |
| dc.subject | translocation | ru |
| dc.subject | neurodevelopmental disorders | ru |
| dc.subject | craniosynostosis | ru |
| dc.subject | syndrome | ru |
| dc.title | Essentially pure partial trisomy 6(p21.31-p25) (case report and literature review) | ru |
| dc.type | Article | ru |
| Appears in Collections: | Т. 7, вып. 4
|
