Wordt geladen...
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...
Bewaard in:
| Gepubliceerd in: | Endocrinol Diabetes Metab Case Rep |
|---|---|
| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Bioscientifica Ltd
2017
|
| Onderwerpen: | |
| Online toegang: | 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 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|