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Deletion 21q22.3 and duplication 7q35q36.3 in a Colombian girl: a case report
BACKGROUND: Genetic disorders are a major cause in the etiology of cases with intellectual disability; however, analysis by a conventional technique such as cytogenetic karyotyping only allows the detection of chromosomal alterations in approximately 9.5 % of cases. The inclusion of new technologies...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2016
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4962380/ https://www.ncbi.nlm.nih.gov/pubmed/27459995 http://dx.doi.org/10.1186/s13256-016-0988-2 |