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Publications by Richard Lao

Novel Mutations in PXDN Cause Microphthalmia and Anterior Segment Dysgenesis

European Journal of Human Genetics

English

Related publications

Mutation Analysis of the Genes Associated With Anterior Segment Dysgenesis, Microcornea and Microphthalmia in 257 Patients With Glaucoma

International Journal of Molecular Medicine

English

Molecular and Developmental Mechanisms of Anterior Segment Dysgenesis

Sensory Systems

English

Foxf2: A Novel Locus for Anterior Segment Dysgenesis Adjacent to the Foxc1 Gene

Multidisciplinary

English

TUBB1 Mutations Cause Thyroid Dysgenesis Associated With Abnormal Platelet Physiology

Yearbook of Paediatric Endocrinology

English

TASP1 Mutation in a Female With Craniofacial Anomalies, Anterior Segment Dysgenesis, Congenital Immunodeficiency and Macrocytic Anemia

Molecular genetics & genomic medicine

Molecular Biology

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What's New in Ocular Anterior Dysgenesis Imaging?

Acta Ophthalmologica

English

Mutations in Mitochondrial Histidyl tRNA Synthetase HARS2 Cause Ovarian Dysgenesis and Sensorineural Hearing Loss of Perrault Syndrome

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

High Resolution Anterior Segment OCT CASIA 2 for Corneal and Anterior Segment Diagnosis

Acta Ophthalmologica

English

AAO 2018 Anterior Segment Section Symposium: Biologic Therapy: Applications in Anterior Segment Disease

Journal of Dry Eye Disease

English