De novo triplication of theMAPTgene from the recurrent 17q21.31 microdeletion region in a patient with moderate intellectual disability and various minor anomalies

Frontotemporal Dementia Phenotype Associated with MAPT Gene Duplication

(2017) Anne Rovelet-Lecrux et al.   JOURNAL OF ALZHEIMERS DISEASE

A copy number variation morbidity map of developmental delay

(2011) Gregory M Cooper et al.   NATURE GENETICS

Recurrent Inversion Events at 17q21.31 Microdeletion Locus Are Linked to the MAPT H2 Haplotype

(2010) P.N. Rao 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

No Evidence of PGRN or MAPT Gene Dosage Alterations in a Collection of Patients with Frontotemporal Lobar Degeneration

(2009) Lena Skoglund et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction

(2009) B Grisart et al.   JOURNAL OF MEDICAL GENETICS

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

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