Loading...
Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event
BACKGROUND: Partial monosomies of chromosome 16q are rare and overlapping effects from complex chromosomal rearrangements often hamper genotype-phenotype correlations for such imbalances. Here, we report the clinical features of an isolated partial monosomy 16q21q22.1 in a boy with a complex de novo...
Na minha lista:
| Main Authors: | , , , , , , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2013
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3737039/ https://ncbi.nlm.nih.gov/pubmed/23915422 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-6-29 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|