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http://cmuir.cmu.ac.th/jspui/handle/6653943832/71586Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Nonglak Boonchooduang | en_US |
| dc.contributor.author | Orawan Louthrenoo | en_US |
| dc.contributor.author | Pranoot Tanpaiboon | en_US |
| dc.date.accessioned | 2021-01-27T03:55:53Z | - |
| dc.date.available | 2021-01-27T03:55:53Z | - |
| dc.date.issued | 2020-10-01 | en_US |
| dc.identifier.issn | 09747559 | en_US |
| dc.identifier.issn | 00196061 | en_US |
| dc.identifier.other | 2-s2.0-85094140380 | en_US |
| dc.identifier.other | 10.1007/s13312-020-2007-3 | en_US |
| dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85094140380&origin=inward | en_US |
| dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/71586 | - |
| dc.description.abstract | © 2020, Indian Academy of Pediatrics. This study describes clinical features of Noonan syndrome and gene mutations, including PTPN11, SOS1, and BRAF in the Thai population. Widely spaced eyes were the most common finding from the digital facial analysis technology used in this study. | en_US |
| dc.subject | Medicine | en_US |
| dc.title | Noonan Syndrome in Thai Children | en_US |
| dc.type | Journal | en_US |
| article.title.sourcetitle | Indian Pediatrics | en_US |
| article.volume | 57 | en_US |
| article.stream.affiliations | Childrens National Health System | en_US |
| article.stream.affiliations | Chiang Mai University | en_US |
| Appears in Collections: | CMUL: Journal Articles | |
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