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Publications by A. Antonell

Evolutionary Mechanisms Shaping the Genomic Structure of the Williams-Beuren Syndrome Chromosomal Region at Human 7q11.23

Genome Research

English

Related publications

Detection of Deletions at 7q11.23 in Williams-Beuren Syndrome by Polymorphic Markers

English

An Atypical 7q11.23 Deletion in a Normal IQ Williams–Beuren Syndrome Patient

European Journal of Human Genetics

English

Metabolic Abnormalities in Williams–Beuren Syndrome

Journal of Medical Genetics

English

"The Impact of Psychiatric Disorders in the Evolution of Patients With Williams-Beuren Syndrome"

BULLETIN OF INTEGRATIVE PSYCHIATRY

English

Human Induced Pluripotent Stem Cell Derived Neurons as a Model for Williams-Beuren Syndrome

Molecular Brain

Molecular Neuroscience

Molecular Biology

English

RNA-Seq Analysis of Gtf2ird1 Knockout Epidermal Tissue Provides Potential Insights Into Molecular Mechanisms Underpinning Williams-Beuren Syndrome

English

Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients

Open Journal of Genetics

English

Negative Autoregulation ofGTF2IRD1in Williams-Beuren Syndrome via a Novel DNA Binding Mechanism

Journal of Biological Chemistry

Molecular Biology

English

Williams-Beuren Syndrome: Cardiovascular Abnormalities in 20 Patients Diagnosed With Fluorescence in Situ Hybridization

Arquivos Brasileiros de Cardiologia

Cardiovascular Medicine

English