A three-dimensional organoid model recapitulates tumorigenic aspects and drug responses of advanced human retinoblastoma von Saengwimol, Duangporn, Rojanaporn, Duangnate, Chaitankar, Vijender, Chittavanich, Pamorn, Aroonroch, Rangsima, Boontawon, Tatpong, Thammachote, Weerin, Jinawath, Natini, Hongeng, Suradej, Kaewkhaw, Rossukon

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1q21.3 deletion involving GATAD2B: An emerging recurrent microdeletion syndrome von Tim‐Aroon, Thipwimol, Jinawath, Natini, Thammachote, Weerin, Sinpitak, Praweena, Limrungsikul, Anchalee, Khongkhatithum, Chaiyos, Wattanasirichaigoon, Duangrurdee

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Clinical delineation of 18q11‐q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects von Rojnueangnit, Kitiwan, Charalsawadi, Chariyawan, Thammachote, Weerin, Pradabmuksiri, Ariya, Tim‐Aroon, Thipwimol, Novelli, Antonio, Loddo, Sara, Briuglia, Silvana, Concetta, Cutrupi M., Wattanasirichaigoon, Duangrurdee, Jinawath, Natini

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LACHT syndrome (Mardini–Nyhan association) with tracheal stenosis in a Thai newborn von Rojnueangnit, Kitiwan, Kositamongkol, Sudatip, Paoin, Wanida, Satdhabudha, Araya, Pharadornuwat, Onsuthi, Wongwandee, Ratthapon, Thammachote, Weerin, Jinawath, Natini

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Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder von Hnoonual, Areerat, Thammachote, Weerin, Tim-Aroon, Thipwimol, Rojnueangnit, Kitiwan, Hansakunachai, Tippawan, Sombuntham, Tasanawat, Roongpraiwan, Rawiwan, Worachotekamjorn, Juthamas, Chuthapisith, Jariya, Fucharoen, Suthat, Wattanasirichaigoon, Duangrurdee, Ruangdaraganon, Nichara, Limprasert, Pornprot, Jinawath, Natini

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LACHT syndrome (Mardini-Nyhan association) with tracheal stenosis in a Thai newborn von Rojnueangnit, Kitiwan, Kositamongkol, Sudatip, Paoin, Wanida, Satdhabudha, Araya, Pharadornuwat, Onsuthi, Wongwandee, Ratthapon, Thammachote, Weerin, Jinawath, Natini

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