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Publications by Linda Nicholson

Observation of a Parental Inversion Variant in a Rare Williams–Beuren Syndrome Family With Two Affected Children

English

Related publications

Metabolic Abnormalities in Williams–Beuren Syndrome

Journal of Medical Genetics

English

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

European Journal of Human Genetics

English

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

Journal of Biological Chemistry

Molecular Biology

English

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

BULLETIN OF INTEGRATIVE PSYCHIATRY

English

De Novo T(X;21)(q28;q11) in a Girl With Phenotypic Features of Williams-Beuren Syndrome.

Journal of Medical Genetics

English

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

English

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

Arquivos Brasileiros de Cardiologia

Cardiovascular Medicine

English

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

Molecular Brain

Molecular Neuroscience

Molecular Biology

English

Determination and Functional Analysis of the Consensus Binding Site for TFII-I Family Member BEN, Implicated in Williams-Beuren Syndrome

Journal of Biological Chemistry

Molecular Biology

English