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Publications by Bassem A. Bejjani

Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia

American Journal of Human Genetics

English

Application of Array-Based Comparative Genomic Hybridization to Clinical Diagnostics

Journal of Molecular Diagnostics

Forensic Medicine

Molecular Medicine

English

Related publications

Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans

Biophysical Journal

English

A Spectrum of CYP1B1 Mutations Associated With Primary Congenital Glaucoma in Families of Pakistani Descent

Human Genome Variation

Molecular Biology

English

Goniodysgenesis Variability and Activity of CYP1B1 Genotypes in Primary Congenital Glaucoma

Multidisciplinary

English

CYP1B1 Mutations in French Patients With Early-Onset Primary Open-Angle Glaucoma

Journal of Medical Genetics

English

Corneal Profile in Primary Congenital Glaucoma

Acta Ophthalmologica

English

Newborn Primary Congenital Glaucoma

Journal of Pediatric Ophthalmology and Strabismus

English

Post Occupancy Evaluation of Primary Schools in Saudi Arabia

Occupational Health

English

ACTN1 Mutations Cause Congenital Macrothrombocytopenia

American Journal of Human Genetics

English

Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

American Journal of Human Genetics

English