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

by Thipwimol Tim-Aroon, Natini Jinawath, Weerin Thammachote, Praweena Sinpitak, Anchalee Limrungsikul, Chaiyos Khongkhatithum, Duangrurdee Wattanasirichaigoon
Published 2018

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

by Kitiwan Rojnueangnit, Sudatip Kositamongkol, Wanida Paoin, Araya Satdhabudha, Onsuthi Pharadornuwat, Ratthapon Wongwandee, Weerin Thammachote, Natini Jinawath
Published 2020

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

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

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

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