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Paper Details

<i>FOXP1</i>-related intellectual disability syndrome: a recognisable entity.
J Med Genet
44
2017
3p deletions, Brain, cardiac and urogenital malformations, FOXP1, FOXP1 defects, FOXP1-related intellectual disability syndrome, ID, MIM: 613670, NMD, Patients, SLI, autistic features, bent downslanting palpebral, blepharophimosis, bulbous nasal tip, facial features, forkhead box protein P1, high broad forehead, intellectual disability, luciferase, neuromotor delay, patients, ptosis, sensorineural hearing loss, specific language impairment
Author NameAffiliation
Guy A RouleauMontreal Neurological Institute, McGill University
Guy A RouleauMontreal Neurological Institute, McGill University
Nicola K RaggeWest Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's Hospital NHS Foundation Trust, Birmingham Women's Hospital
Pablo LapunzinaInstituto de Genetica Medica y Molecular, Hospital Universitario La Paz
Jonathan SebatBeyster Center for Genomics of Psychiatric Diseases, University of California
Jonathan SebatBeyster Center for Genomics of Psychiatric Diseases, University of California
Keith K Vauxuniversity of california san diego School of Medicine
Bruno DallapiccolaBambino Gesu Children's Hospital, IRCCS
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