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Chromosome 1p31.1 Deletion Syndrome: Limited Expression
Chromosomal microdeletion syndromes usually present with neurological abnormalities, developmental delays, and various systemic abnormalities. 1p31 microdeletion syndrome is one of the novel microdeletion syndromes that usually presents with developmental delay, intellectual disability, various cran...
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| Udgivet i: | Ann Indian Acad Neurol |
|---|---|
| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Wolters Kluwer - Medknow
2021
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8061518/ https://ncbi.nlm.nih.gov/pubmed/33911383 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/aian.AIAN_258_20 |
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