Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Imen Rejeb

The First Missense Mutation of NHS Gene in a Tunisian Family With Clinical Features of NHS Syndrome Including Cardiac Anomaly

European Journal of Human Genetics
Genetics
2011English

Related publications

A Family With a New Elastin Gene Mutation: Broad Clinical Spectrum, Including Sudden Cardiac Death

Cardiology in the Young
PediatricsCardiologyPerinatologyCardiovascular MedicineMedicineChild Health
2010English

Identification of the Gene for Nance-Horan Syndrome (NHS)

Journal of Medical Genetics
Genetics
2004English

Clinical Pharmacology in the NHS

Journal of the Royal Society of Medicine
Medicine
1979English

How Reliable Are Clinical Systems in the UK NHS? A Study of Seven NHS Organisations

BMJ Quality and Safety
MedicineHealth Policy
2012English

Novel Splice Site IDUA Gene Mutation in Tunisian Pedigrees With Hurler Syndrome

Diagnostic Pathology
Forensic MedicineMedicinePathologyHistology
2018English

A Novel Missense Mutation in the CYLD Gene in a Spanish Family With Multiple Familial Trichoepithelioma

Archives of Dermatology
2007English

NHS Managers and Clinical Management

Psychiatric Bulletin
1992English

Long QT Syndrome With Nocturnal Cardiac Events Caused by a KCNH2 Missense Mutation (G604S)

Internal Medicine
Internal MedicineMedicine
2012English

Restructuring of HR Practices in NHS: A Case Study of Oxleas NHS

International Journal of Economics & Management Sciences
2015English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy