References
- VeltmanJAGenomic microarrays in clinical diagnosisCurr Opin Pediatr200618659860317099357
- SlavotinekAMNovel microdeletion syndromes detected by chromosome microarraysHum Genet2008124111718512078
- VissersLELMde LigtJGilissenCA de novo paradigm for mental retardationNat Genet201042121109111221076407
- BattagliaANovelliABernardiniLIgliozziRParriniBFurther characterization of the new microdeletion syndrome of 16p11.2–p12.2Am J Med Genet2009149A61200120419449418
- Barge-SchaapveldDQMaasSMPolstraAKnegtLCHennekamRCThe atypical 16p11.2 deletion: a not so atypical microdeletion syndrome?Am J Med Genet A2011155A51066107221465664
- WeissLAShenYKornJMAutism ConsortiumAssociation between microdeletion and microduplication at 16p11.2 and autismN Engl J Med2008358766767518184952
- SampsonMGCoughlinCRKaplanPEvidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung diseaseAm J Med Genet2010152A102618262220799338
- HansonENasirRHFongA16p11.2 Study Group CliniciansCognitive and behavioural characterization of 16p11.2 deletion syndromeJ Dev Behav Pediatr201031864965720613623
- CrepelASteyaertJDe la MarcheWNarrowing the critical deletion region for autism spectrum disorders on 16p11.2Am J Med Genet2011156224324521302354
- ZuffereyFSherrEHBeckmannNDSimons VIP Consortium; 16p11.2 European Consortium. A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disordersJ Med Genet2012491066066823054248
- Bachmann-GageskuRMeffordHCCowanCRecurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesityGenet Med2010121064164720808231
- BochukovaEGHuangNKeighJLarge, rare chromosomal deletions associated with severe early-onset obesityNature2010463728166667019966786
- WaltersRGJacquemontSValsesiaAA novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2Nature2010463728167167520130649
- KaufmanSKaufmanNLMulderJLDekkerRDekkerPHDutch Adaptation of the Kaufman Adolescent and Adult Intelligence TestAmsterdamPearson2004
- van der HeijdenPTEggerJIDerksenJJPsychometric evaluation of the MMPI-2 Restructured Clinical scales in two Dutch samplesJ Pers Assess200890545646418704804
- GuhaSReesEDarvasiAMolecular Genetics of Schizophrenia Consortium; Wellcome Trust Case Control Consortium 2. Implication of a rare deletion at distal 16p11.2 in schizophreniaJAMA Psychiatry201370325326023325106
- CooperGMCoeBPGirirajanSA copy number variation morbidity map of developmental delayNat Genet201143983884621841781
- KirovGPocklingtonAJHolmansPDe novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophreniaMol Psychiatr2012172140153
- FirthHVRichardsSMBevanAPDECIPHER: Database of chromosomal imbalance and phenotype in humans using ensemble resourcesAm J Hum Genet200984452453319344873