COFFIN-SIRIS SYNDROME 1; CSS1

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Summary

Literature (1)

Literature for OMIM 135900: COFFIN-SIRIS SYNDROME 1; CSS1

Xenbase Articles:
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Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome., Pagnamenta AT,Blyth M,McConnell V,Ikegawa S,Matsumoto N,Lo-Castro A,Plessis G,Albrecht B,Taylor JC,Howard MF,Keays D,Kühl SJ,Kini U,McNeill A,Mansour S,Tsurusaki Y,Battaglia A,Kou I,Sohal AS,Hempel A, J Med Genet. March 1, 2016; 53(3):1468-6244.

Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome., Pagnamenta AT,Blyth M,McConnell V,Ikegawa S,Matsumoto N,Lo-Castro A,Plessis G,Albrecht B,Taylor JC,Howard MF,Keays D,Kühl SJ,Kini U,McNeill A,Mansour S,Tsurusaki Y,Battaglia A,Kou I,Sohal AS,Hempel A, J Med Genet. March 1, 2016; 53(3):1468-6244.