Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0) Francesco Vetrini , Shane McKee , Jill A. Rosenfeld , Mohnish Suri , Andrea M. Lewis , Kimberly Nugent , Elizabeth Roeder , Rebecca O. Littlejohn , Sue Holder , Wenmiao Zhu , Joseph T. Alaimo , Brett H. Graham , Jill M. Harris , James B. Gibson , Matthew Pastore , Kim L. McBride , Makanko Komara , Lihadh Al-Gazali , Aisha Al Shamsi , Elizabeth A. Fanning , Klaas J. Wierenga , Daryl A. Scott , Ziva Ben-Neriah , Vardiella Meiner , Hanoch Cassuto , Orly Elpeleg , J. Lloyd Holder , Lindsay C. Burrage , Laurie H. Seaver , Lionel Van Maldergem , Sonal Mahida , Janet S. Soul , Margaret Marlatt , Ludmila Matyakhina , Julie Vogt , June Anne Gold , Soo Mi Park , Vinod Varghese , Anne K. Lampe , Ajith Kuttannair Kumar , Melissa Lees , Muriel Holder-Espinasse , Vivienne McConnell , Birgitta Bernhard , Ed Blair , Victoria Harrison , Donna M. Muzny , Richard A. Gibbs , Sarah H. Elsea , Jennifer E. Posey , Weimin Bi , Seema R. Lalani , Fan Xia , Yaping Yang , Christine M. Eng , James R. Lupski , Pengfei Liu Genome Medicine(2019)
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