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Publications by Ines Ouertani

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

Open Journal of 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

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

Arquivos Brasileiros de Cardiologia

Cardiovascular Medicine

English

Challenges in Clinical Diagnosis of Williams-Beuren Syndrome in Sub-Saharan Africans: Case Reports From Cameroon

Molecular Syndromology

English

A Clinical, Cytogenetic, and Molecular Study of 40 Adults With the Prader-Willi Syndrome.

Journal of Medical Genetics

English

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

English

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

English

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

Journal of Biological Chemistry

Molecular Biology

English

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

European Journal of Human Genetics

English