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

Open Journal of Genetics
doi 10.4236/ojgen.2014.45036
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Scientific Research Publishing, Inc,

Related search

Metabolic Abnormalities in Williams–Beuren Syndrome

Journal of Medical Genetics
Genetics
2015English

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

BULLETIN OF INTEGRATIVE PSYCHIATRY
2020English

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

Arquivos Brasileiros de Cardiologia
Cardiovascular MedicineCardiology
2003English

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

Molecular Syndromology
Genetics
2014English

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

Journal of Medical Genetics
Genetics
1995English

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

Clinics
Medicine
2011English

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

BMC Genomics
BiotechnologyGenetics
2016English

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

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2009English

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

European Journal of Human Genetics
Genetics
2009English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy