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Huriez syndrome: Additional pathogenic variants supporting allelism to
SMARCAD
syndrome
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| | Abigail Y. T. Loh, Sanja Špoljar, Granville Y. W. Neo, Nathalie Escande-Beillard, Marc Leushacke, Monique N. H. Luijten, Byrappa Venkatesh, Carine Bonnard, Maurice A. M. Steensel, Henning Hamm, Andrew Carmichael, Neil Rajan, Thomas J. Carney, Bruno Reversade | | | American Journal of Medical Genetics Part A. 2022; | | | [Pubmed] [Google Scholar] [DOI] | |
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