POU3F3‐related Disorder: Defining the Phenotype and Expanding the Molecular SpectrumAlessandra Rossi,Lot Snijders Blok,Sonja Neuser,Chiara Kloeckner,Konrad Platzer,Laurence Olivier Faivre,Heike Weigand,Maria L. Dentici,Marco Tartaglia,Marcello Niceta,Paolo Alfieri,Siddharth Srivastava,David Coulter,Lacey Smith,Kristin Vinorum,Gerarda Cappuccio,Nicola Brunetti-Pierri,Deniz Torun,Mutluay Arslan,Mathilde F. Lauridsen,Oliver Murch,Rachel Irving,Sally A. Lynch,Sarju G. Mehta,Jenny Carmichael,Evelien Zonneveld-Huijssoon,Bert de Vries,Tjitske Kleefstra,Katrine M. Johannesen, Ian T. Westphall,Susan S. Hughes,Sarah Smithson,Julie Evans,Tracy Dudding-Byth,Marleen Simon,Ellen van Binsbergen,Johanna C. Herkert,Gea Beunders,Henry Oppermann,Mert Bakal,Rikke S. Moller,Guido Rubboli,Allan BayatCLINICAL GENETICS（2023）引用 2|浏览8关键词autism,cupped ears,epilepsy,neurodevelopmental disorderAI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
