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Publications by I. Fadl Elmula

Molecular Cytogenetic Study of the Nf2 Gene Deletion in Meningioma in Sudanese Patients

Balkan Journal of Medical Genetics

English

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The Evaluation of DiGeorge Syndrome Gene Deletion Using Molecular Cytogenetic Techniques

English

Study of Six Patients With Complete F9 Deletion Characterized by Cytogenetic Microarray: Role of the SOX3 Gene in Intellectual Disability

Journal of Thrombosis and Haemostasis

English

Molecular Cytogenetic Evaluation of Xq Deletion Mosaicism in a Case of Primary Amenorrhea

International Journal of Human Genetics

English

Angiotensinogen Gene Polymorphism (M235t) in Sudanese Hypertensive Patients.

International Journal of Advanced Research

English

Clinical Implications of Cytogenetic Heterogeneity in Multiple Myeloma Patients With TP53 Deletion

Modern Pathology

Forensic Medicine

English

Association of NOS3 Gene Polymorphisms With Essential Hypertension in Sudanese Patients: A Case Control Study

BMC Medical Genetics

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

Open Journal of Genetics

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Molecular Study of the Rhodopsin Gene in Retinitis Pigmentosa Patients in the Basque Country.

Journal of Medical Genetics

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Neuron-Specific Deletion of the Nf2 Tumor Suppressor Impairs Functional Nerve Regeneration

Multidisciplinary

English