Cargando…
Phenotypic variability in a Hungarian patient with the 4q21 microdeletion syndrome
BACKGROUND: Interstitial deletions of 4q21 (MIM 613509) have already been reported in more than a dozen patients with deletions ranging from 2 to 15.1 Mb delineating a common phenotype including marked growth restriction, hypotonia, severe developmental delay with absent or delayed speech and distin...
| Autores principales: | , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2015
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359765/ https://www.ncbi.nlm.nih.gov/pubmed/25774221 http://dx.doi.org/10.1186/s13039-015-0118-7 |