Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/71586
Title: Noonan Syndrome in Thai Children
Authors: Nonglak Boonchooduang
Orawan Louthrenoo
Pranoot Tanpaiboon
Authors: Nonglak Boonchooduang
Orawan Louthrenoo
Pranoot Tanpaiboon
Keywords: Medicine
Issue Date: 1-Oct-2020
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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85094140380&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/71586
ISSN: 09747559
00196061
Appears in Collections:CMUL: Journal Articles

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