heterozygous protein-truncating variants cause a recognizable syndrome with intellectual disability and distinctive facial gestalt : A study to clarify the HIST 1 H 1 E syndrome phenotype in 30 individuals
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C. Cytrynbaum | R. Weksberg | J. Graham | H. Stewart | Rachel H Horton | S. Banka | M. Lees | F. Stewart | L. Faivre | M. McDonald | B. Skotko | D. Amor | Clare L. Allen | D. Shears | C. Coubes | A. Ardissone | P. Mark | K. Tatton-Brown | C. Loveday | D. Kotzot | H. Luk | R. Verdugo | A. McConkie-Rosell | J. Pappas | Y. Zarate | A. Zachariou | K. Low | G. Lay-Son | D. Burkardt | Alexia Bourgois | Gerard Marion | Christophe Phillipe
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