The Immune Status of Patients with 16p11.2 Deletion Syndrome

16p11.2 deletion syndrome

(2021) Wendy K Chung et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Rare variants at 16p11.2 are associated with common variable immunodeficiency

(2015) S. Melkorka Maggadottir et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

(2010) Ruxandra Bachmann-Gagescu et al.   GENETICS IN MEDICINE

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

(2009) B. A. Fernandez et al.   JOURNAL OF MEDICAL GENETICS

Severe combined immunodeficiency (SCID) and attention deficit hyperactivity disorder (ADHD) associated with a coronin-1A mutation and a chromosome 16p11.2 deletion

(2008) Lawrence R. Shiow et al.   CLINICAL IMMUNOLOGY

Association between Microdeletion and Microduplication at 16p11.2 and Autism

(2008) Lauren A. Weiss et al.   NEW ENGLAND JOURNAL OF MEDICINE