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Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2006, Volume 140A, Issue 19, pp. 2063 - 2074
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 09/2005, Volume 42, Issue 9, pp. 699 - 705
Journal Article
Genetic Testing and Molecular Biomarkers, ISSN 1945-0265, 05/2012, Volume 16, Issue 5, pp. 412 - 417
Journal Article
Human Mutation, ISSN 1059-7794, 2011, Volume 32, Issue 7, pp. 853 - 859
The core phenotype of Kleefstra syndrome (KS) is characterized by intellectual disability, childhood hypotonia, and a characteristic facial appearance. This... 
chromosome 9q | EHMT1 | subtelomere deletion | 9qSTDS | Kleefstra syndrome | Chromosome 9q | Subtelomere deletion | MECP2 | SUBTELOMERIC DELETION SYNDROME | GENETICS & HEREDITY | MICRODELET