Williams syndrome and the Elastin gene in Thai patients
Williams syndrome (WS) has long been known as a complex disorder of dysmorphic facial features, described as elfin face, mental retardation or learning disability, loquacious personality, and supravalvular aortic stenosis. The etiology is now known to be due to deletion of the elastin gene (ELN) on...
Saved in:
Main Authors: | Nichara Ruangdaraganon, Chintana Tocharoentanaphol, Nittaya Kotchabhakdi, Pongsak Khowsathit |
---|---|
Other Authors: | Mahidol University |
Format: | Article |
Published: |
2018
|
Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/25745 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Mahidol University |
Similar Items
-
Chromosome 22q11 deletion syndrome : The first three cases reported in Thailand
by: Nichara Ruangdaraganon, et al.
Published: (2018) -
Prevalence and clinical characteristics of fragile X syndrome at Child Development Clinic, Ramathibodi Hospital
by: Nichara Ruangdaraganon, et al.
Published: (2018) -
Chromosome 22q11 deletions in patients with conotruncal heart defects
by: A. Khositseth, et al.
Published: (2018) -
William-Beuren Syndrome: Comprehensive Dental Care in Child Patient
by: Naila Marzuqi, -, et al.
Published: (2022) -
Metopic and Sagittal Craniosynostosis in Williams Syndrome
by: Chaisrisawadisuk S.
Published: (2023)