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https://hdl.handle.net/11000/37755Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Ochando, Isabel | - |
| dc.contributor.author | Alonzo Martínez, Melanie Cristine | - |
| dc.contributor.author | Serrano, Ana María | - |
| dc.contributor.author | Urbano, Antonio | - |
| dc.contributor.author | Cazorla, Eduardo | - |
| dc.contributor.author | Calvo, Dolores | - |
| dc.contributor.author | Rueda, Joaquín | - |
| dc.contributor.other | Departamentos de la UMH::Histología y Anatomía | es_ES |
| dc.date.accessioned | 2025-10-31T09:40:33Z | - |
| dc.date.available | 2025-10-31T09:40:33Z | - |
| dc.date.created | 2018-07 | - |
| dc.identifier.citation | The application of clinical genetics. 2018 Jul 3:11:77-80 | es_ES |
| dc.identifier.issn | 1178-704X | - |
| dc.identifier.uri | https://hdl.handle.net/11000/37755 | - |
| dc.description.abstract | Reported cases of distal 15q interstitial duplications are uncommon and do not result in a recognizable pattern of abnormalities. Some studies report prenatal overgrowth, while others describe growth retardation. We present molecular cytogenetic characterization of a 14 Mb interstitial duplication, encompassing 81 Online Mendelian Inheritance in Man (OMIM) genes, in a fetus with single umbilical artery and short limbs. We propose that growth restriction, previously described and present in our patient, may be due to duplication of a gene or genes contained in the 15q24 region. | es_ES |
| dc.format | application/pdf | es_ES |
| dc.format.extent | 4 | es_ES |
| dc.language.iso | eng | es_ES |
| dc.publisher | Taylor and Francis. Group Dove Press | es_ES |
| dc.rights | info:eu-repo/semantics/openAccess | es_ES |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
| dc.subject | distal 15q trisomy | es_ES |
| dc.subject | prenatal diagnosis | es_ES |
| dc.subject | short limbs | es_ES |
| dc.subject.other | CDU::6 - Ciencias aplicadas::61 - Medicina | es_ES |
| dc.title | Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 15q24.3-q26.1 | es_ES |
| dc.type | info:eu-repo/semantics/article | es_ES |
| dc.relation.publisherversion | https://doi.org/10.2147/TACG.S159377 | es_ES |

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