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SUN-064 Diversity of Endocrine Function in Patients with CHARGE Association
Context: CHARGE association consists of congenital malformation of Coloboma, Heart defect, Atresia choanae, Retarded growth and development, Genital hypoplasia, Ear anomalies and/or deafness. It is often caused by CHD7 gene mutation, which also one of the causative gene for Kallmann syndrome. The en...
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| Publicado no: | J Endocr Soc |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7209718/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.891 |
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