Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

17q21.31 Microdeletion Syndrome: Further Expanding the Clinical Phenotype

(2010) F.H. Sharkey et al.   CYTOGENETIC AND GENOME RESEARCH

Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients with mental retardation

(2010) Christèle Dubourg et al.   European Journal of Medical Genetics

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Subunit Composition and Substrate Specificity of a MOF-containing Histone Acetyltransferase Distinct from the Male-specific Lethal (MSL) Complex

(2009) Yong Cai et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome

(2009) T Y Tan et al.   JOURNAL OF MEDICAL GENETICS

Two Mammalian MOF Complexes Regulate Transcription Activation by Distinct Mechanisms

(2009) Xiangzhi Li et al.   MOLECULAR CELL