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Publications by Habiba Chaabouni Bouhamed
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
Single-Cell Genetic Analysis Validates Cytopathological Identification of Circulating Cancer Cells in Patients With Clear Cell Renal Cell Carcinoma
Oncotarget
Oncology
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A Family With a New Elastin Gene Mutation: Broad Clinical Spectrum, Including Sudden Cardiac Death
Cardiology in the Young
Pediatrics
Cardiology
Perinatology
Cardiovascular Medicine
Medicine
Child Health
Identification of the Gene for Nance-Horan Syndrome (NHS)
Journal of Medical Genetics
Genetics
Clinical Pharmacology in the NHS
Journal of the Royal Society of Medicine
Medicine
How Reliable Are Clinical Systems in the UK NHS? A Study of Seven NHS Organisations
BMJ Quality and Safety
Medicine
Health Policy
Novel Splice Site IDUA Gene Mutation in Tunisian Pedigrees With Hurler Syndrome
Diagnostic Pathology
Forensic Medicine
Medicine
Pathology
Histology
A Novel Missense Mutation in the CYLD Gene in a Spanish Family With Multiple Familial Trichoepithelioma
Archives of Dermatology
NHS Managers and Clinical Management
Psychiatric Bulletin
Long QT Syndrome With Nocturnal Cardiac Events Caused by a KCNH2 Missense Mutation (G604S)
Internal Medicine
Internal Medicine
Medicine
Restructuring of HR Practices in NHS: A Case Study of Oxleas NHS
International Journal of Economics & Management Sciences