A carregar...
MR Imaging Findings in Xp21.2 Duplication Syndrome
Xp21.2 duplication syndrome is a rare genetic disorder of undetermined prevalence and clinical relevance. As the use of chromosomal microarray has become first line for the work-up of childhood developmental delay, more gene deletions and duplications have been recognized. To the best of our knowled...
Na minha lista:
| Publicado no: | J Radiol Case Rep |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
EduRad
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5065289/ https://ncbi.nlm.nih.gov/pubmed/27761175 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3941/jrcr.v10i5.2563 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|