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Paper Details

CMIP haploinsufficiency in two patients with autism spectrum disorder and co-occurring gastrointestinal issues.
Am J Med Genet A
6
2017
16q23, 16q23.2q23, 280kb de, 517kb deletion, ASD, Autism spectrum disorder, CMIP, CMIP gene, CMIP haploinsufficiency, Patient, SLI, autism spectrum disorder, causative gene, developmental delay, gastrointestinal, gastrointestinal issues, impairments, patient, patients, specific language impairment, susceptibility locus, syndromic ASD
Author NameAffiliation
Minjie LuoThe Children's Hospital of Philadelphia
Minjie LuoPerelman School of Medicine at the University of Pennsylvania
Minjie LuoThe Children's Hospital of Philadelphia
Minjie LuoPerelman School of Medicine at the University of Pennsylvania
Margaret HarrThe Children's Hospital of Philadelphia
Elaine H ZackaiThe Children's Hospital of Philadelphia
Elaine H ZackaiPerelman School of Medicine at the University of Pennsylvania
Nancy B SpinnerThe Children's Hospital of Philadelphia
Nancy B SpinnerPerelman School of Medicine at the University of Pennsylvania
Laura K ConlinThe Children's Hospital of Philadelphia
Laura K ConlinPerelman School of Medicine at the University of Pennsylvania
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Release 1.2