Llwytho...
Congenital hyperinsulinism and Poland syndrome in association with 10p13–14 duplication
SUMMARY: Poland syndrome (PS) is a rare congenital condition, affecting 1 in 30 000 live births worldwide, characterised by a unilateral absence of the sternal head of the pectoralis major and ipsilateral symbrachydactyly occasionally associated with abnormalities of musculoskeletal structures. A ba...
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| Cyhoeddwyd yn: | Endocrinol Diabetes Metab Case Rep |
|---|---|
| Prif Awduron: | , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Bioscientifica Ltd
2017
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5404473/ https://ncbi.nlm.nih.gov/pubmed/28458900 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-16-0125 |
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