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Publications by Feras M Hantash

A Large Deletion in the CFTR Gene in CBAVD

Genetics in Medicine

English

Development of a Novel, Accurate, Automated, Rapid, High-Throughput Technique Suitable for Population-Based Carrier Screening for Fragile X Syndrome

Genetics in Medicine

English

Related publications

A Large PROP1 Gene Deletion in a Turkish Pedigree

Case Reports in Endocrinology

English

A Novel Double Deletion Underscores the Importance of Characterizing End Points of the CFTR Large Rearrangements

European Journal of Human Genetics

English

CFTR Gene Transfer and Tracking the CFTR Protein in the Airway Epithelium

English

Dominantly Inherited Distal Nemaline/Cap Myopathy Caused by a Large Deletion in the Nebulin Gene

Neuromuscular Disorders

English

A Wide Methodological Approach to Identify a Large Duplication in CFTR Gene in a CF Patient Uncharacterised by Sequencing Analysis

Journal of Cystic Fibrosis

Respiratory Medicine

English

Further Delineation of the Phenotype Caused by a Novel Large Homozygous Deletion of GRID2 Gene in an Adult Patient

Clinical Case Reports

English

Large Deletion in PIGL: A Common Mutational Mechanism in CHIME Syndrome?

Genetics and Molecular Biology

Molecular Biology

English

Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.

Journal of Medical Genetics

English

Apparent Homozygosity of p.Phe508del inCFTRdue to a Large Gene Deletion of Exons 4–11

Case Reports in Genetics

English