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Publications by Brittany Hines

IPEX Syndrome in Siblings With a Novel Variant in FOXP3

Journal of Allergy and Clinical Immunology

English

Related publications

IPEX Syndrome, FOXP3 and Cancer

Journal of Syndromes

English

Somatic and Germline FOXP3 Mosaicism in the Mother of a Boy With IPEX Syndrome

European Journal of Immunology

English

IPEX as a Result of Mutations in FOXP3

Clinical and Developmental Immunology

English

A Rare ANOS1 Variant in Siblings With Kallmann Syndrome Identified by Whole Exome Sequencing

Reproductive Medicine

English

Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation

Journal of Ultrasound in Medicine

Nuclear Medicine

Ultrasound Technology

English

Lentiviral Gene Therapy in HSCs Restores Lineage-Specific Foxp3 Expression and Suppresses Autoimmunity in a Mouse Model of IPEX Syndrome

Molecular Medicine

English

Hyperimmunoglobulinaemia D Syndrome in India: Report of Two Siblings With a Novel Mutation

Annals of the Rheumatic Diseases

Molecular Biology

English

Glaucoma in Siblings With Morquio Syndrome.

British Journal of Ophthalmology

Molecular Neuroscience

Sensory Systems

English

Mild Clinical Features of Isolated Methylmalonic Acidemia Associated With a Novel Variant in the MMAA Gene in Two Chinese Siblings

BMC Medical Genetics

English