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Publications by Fred Gilbert

Novel 47.5-Kb Deletion in RAB27A Results in Severe Griscelli Syndrome Type 2

Molecular Genetics and Metabolism

Molecular Biology

English

Related publications

A Novel Missense Mutation (G43S) in the Switch I Region of Rab27A Causing Griscelli Syndrome

Molecular Genetics and Metabolism

Molecular Biology

English

Griscelli Syndrome Type 2: Long-Term Follow-Up After Unrelated Donor Bone Marrow Transplantation

English

Cellular and Clinical Report of New Griscelli Syndrome Type III Cases

Pigment Cell and Melanoma Research

Molecular Biology

English

Haemophagocytic Lymphohistiocytosis and Silvery Hair in Griscelli Syndrome

British Journal of Haematology

English

Identification of a Novel Deletion in UDP-glucuronosyltransferase Gene in a Patient With Crigler–Najjar Syndrome Type I

Blood Cells, Molecules, and Diseases

Molecular Medicine

Molecular Biology

English

Adenovirus Type 2 DNA Replicated in Arginine-Starved KB Cells Is Infectious

Journal of Virology

English

Intragenic Deletion as a Novel Type of Mutation in Wolman Disease

Molecular Genetics and Metabolism

Molecular Biology

English

Novel In-Frame FLNB Deletion Causes Larsen Syndrome in a Three-Generation Pedigree

Cold Spring Harbor molecular case studies

Molecular Medicine

English

Severe Conjunctivochalasis in Association With Classic Type Ehlers-Danlos Syndrome

BMC Ophthalmology

English