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Publications by J Feingold

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

Journal of Medical Genetics

English

Related publications

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

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

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

English

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

Arquivos Brasileiros de Cardiologia

Cardiovascular Medicine

English

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

Journal of Biological Chemistry

Molecular Biology

English

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

Open Journal of Genetics

English

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

Molecular Brain

Molecular Neuroscience

Molecular Biology

English