7q11.23 Duplication syndrome: Physical characteristics and natural history

Children with 7q11.23 duplication syndrome: Psychological characteristics

(2015) Carolyn B. Mervis et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Aortopathy in the 7q11.23 microduplication syndrome

(2014) Ashley Parrott et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Cardiovascular and genitourinary anomalies in patients with duplications within the Williams syndrome critical region: Phenotypic expansion and review of the literature

(2014) Yuri A. Zarate et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

(2013) Jennifer Gladys Mulle et al.   BIOLOGICAL PSYCHIATRY

Duplication of GTF2I Results in Separation Anxiety in Mice and Humans

(2012) Carolyn B. Mervis et al.   AMERICAN JOURNAL OF HUMAN GENETICS

7q11.23 Microduplication: a recognizable phenotype

(2012) A Dixit et al.   CLINICAL GENETICS

Autistic Disorder in Patients with Williams-Beuren Syndrome: A Reconsideration of the Williams-Beuren Syndrome Phenotype

(2012) Sylvie Tordjman et al.   PLoS One

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

(2011) Stephan J. Sanders et al.   NEURON

Long-Term Outcomes of Patients With Cardiovascular Abnormalities and Williams Syndrome

(2010) R. Thomas Collins et al.   AMERICAN JOURNAL OF CARDIOLOGY

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome

(2010) Holly H. Hobart et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Incidence of diverticular disease and complicated diverticular disease in young patients with Williams syndrome

(2010) Stefano Stagi et al.   PEDIATRIC SURGERY INTERNATIONAL

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome

(2009) Nathalie Van der Aa et al.   European Journal of Medical Genetics

Further clinical description of duplication of Williams–Beuren region presenting with congenital glaucoma and brachycephaly

(2008) J.L. Merritt et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The common inversion of the Williams–Beuren syndrome region at 7q11.23 does not cause clinical symptoms

(2008) Elaine Tam et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion

(2008) Claudia Torniero et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical variability of the 22q11.2 duplication syndrome

(2008) Christian Wentzel et al.   European Journal of Medical Genetics