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Infantile presentation of 3q26.33-3q27.2 deletion syndrome
A very rare syndrome, 3q26.33-3q27. 2 microdeletion, has only been described in seven case reports previously, all of which highlight genotypic and phenotypic variations of the presentations identified in school-aged and adolescent children. The patients in these cases had varying sized deletions bu...
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| Gepubliceerd in: | BMJ Case Rep |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BMJ Publishing Group
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7705523/ https://ncbi.nlm.nih.gov/pubmed/33257348 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-233215 |
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