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Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2019, Volume 104, Issue 4, pp. 758 - 766
By using exome sequencing and a gene matching approach, we identified and inherited pathogenic variants in in 14 unrelated individuals and three affected... 
leukemia | KDM3B | lymphoma | developmental delay | short stature | cancer predisposition | facial recognition | intellectual disability | DEMETHYLASE KDM3B | INDIVIDUALS | RUBINSTEIN-TAYBI SYNDROME | PROTEIN | GENETICS | GENETICS & HEREDITY | MYELOID-LEUKEMIA | JMJD1C | MUTATIONS | WEAVER SYNDROME | DELETION | Genetic aspects | Research | Genetic variation | Mental retardation | Risk factors | Exome sequencing | Report
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 08/2017, Volume 18, Issue 8, p. 1820
Journal Article
Journal Article
Pediatrics, ISSN 0031-4005, 01/2009, Volume 123, Issue 1, pp. 391 - 398
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2006, Volume 355, Issue 8, pp. 788 - 798
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2014, Volume 9, Issue 2, p. e89749
Journal Article
Scientific reports, ISSN 2045-2322, 10/2018, Volume 8, Issue 1, pp. 15845 - 1
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has not been fixed in the paper. 
Genomes | Next-generation sequencing
Journal Article