Browsing by Author "Le Caignec, C"
Now showing items 1-2 of 2
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A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
Walters, RG; Jacquemont, S; Valsesia, A; de Smith, AJ; Martinet, D; Andersson, J; Falchi, M; Chen, F; Andrieux, J; Lobbens, S (2010-02-04) -
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas.
Tolchin, D; Yeager, JP; Prasad, P; Dorrani, N; Russi, AS; Martinez-Agosto, JA; Haseeb, A; Angelozzi, M; Santen, GWE; Ruivenkamp, C (2020-06-04)SOX6 belongs to a family of 20 SRY-related HMG-box-containing (SOX) genes that encode transcription factors controlling cell fate and differentiation in many developmental and adult processes. For SOX6, these processes ...