Llwytho...
Prader–Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion
We report a 17-year-old boy who met most of the major Prader–Willi syndrome (PWS) diagnostic criteria, including infantile hypotonia and poor feeding followed by hyperphagia, early-onset morbid obesity, delayed development, and characteristic facial features. However, unlike many children with PWS,...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Genes (Basel) |
|---|---|
| Prif Awduron: | , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
MDPI
2020
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7073628/ https://ncbi.nlm.nih.gov/pubmed/31991769 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11020128 |
| Tagiau: |
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