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Wiley, The American Journal of Medical Genetics - Part A, 10(179), p. 2049-2055, 2019

DOI: 10.1002/ajmg.a.61321

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HIST1H1E heterozygous protein‐truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt: A study to clarify the HIST1H1E syndrome phenotype in 30 individuals

Journal article published in 2019 by Yuri A. Zarate ORCID, Deepika D'Cunha Burkardt ORCID, Allyn McConkie‐Rosell, Marie McDonald, Anna Zachariou, John Pappas ORCID, Christophe Phillipe, Deborah Shears, Brian Skotko, Fiona Stewart, Helen Stewart ORCID, I. Karen Temple, Ricardo A. Verdugo, Rosanna Weksberg ORCID, Chey Loveday and other authors.
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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