1q21.3 deletion involving GATAD2B: An emerging recurrent microdeletion syndrome

بواسطة Thipwimol Tim-Aroon, Natini Jinawath, Weerin Thammachote, Praweena Sinpitak, Anchalee Limrungsikul, Chaiyos Khongkhatithum, Duangrurdee Wattanasirichaigoon
منشور في 2018

LACHT syndrome (Mardini–Nyhan association) with tracheal stenosis in a Thai newborn

بواسطة Kitiwan Rojnueangnit, Sudatip Kositamongkol, Wanida Paoin, Araya Satdhabudha, Onsuthi Pharadornuwat, Ratthapon Wongwandee, Weerin Thammachote, Natini Jinawath
منشور في 2020

A three-dimensional organoid model recapitulates tumorigenic aspects and drug responses of advanced human retinoblastoma

بواسطة Duangporn Saengwimol, Duangnate Rojanaporn, Vijender Chaitankar, Pamorn Chittavanich, Rangsima Aroonroch, Tatpong Boontawon, Weerin Thammachote, Natini Jinawath, Suradej Hongeng, Rossukon Kaewkhaw
منشور في 2019

Clinical delineation of 18q11-q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects

بواسطة Kitiwan Rojnueangnit, Chariyawan Charalsawadi, Weerin Thammachote, Ariya Pradabmuksiri, Thipwimol Tim-Aroon, Antonio Novelli, Sara Loddo, Silvana Briuglia, Cutrupi M. Concetta, Duangrurdee Wattanasirichaigoon, Natini Jinawath
منشور في 2020