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De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome

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Description scientific article published on 28 February 2019
Author/s

author: Jennifer E. Posey  Klaas J. Wierenga  Jill A Rosenfeld  Ludmila Matyakhina  Vivienne McConnell  Kimberly Margaret Nugent  Wenmiao Zhu  Mohnish Suri  June-Anne Gold  Ziva Ben-Neriah  Makanko Komara  Hanoch Cassuto  Margaret Marlatt  DDD study  Birgitta Bernhard  Yaping Yang  Richard A Gibbs  Christine M. Eng  Francesco Vetrini  James R. Lupski  Lionel Van Maldergem  Shane McKee  Donna Muzny 

Publication date February 28, 2019
Language English
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