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Publications by R. E. Oakey

Cloning of a cDNA for Steroid Sulfatase: Frequent Occurrence of Gene Deletions in Patients With Recessive X Chromosome-Linked Ichthyosis.

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

Multidisciplinary

1987

English

Related publications

Increased Prevalence of Filaggrin Deficiency in 51 Patients With Recessive X-Linked Ichthyosis Presenting for Dermatological Examination

Journal of Investigative Dermatology

English

Comparing Histopathology From Patients With X-Linked Recessive Ichthyosis and Autosomal Recessive Congenital Ichthyosis With Transglutaminase 1 Mutation: A Report From the National Registry for Ichthyosis and Related Skin Disorders

Journal of the American Academy of Dermatology

Dermatology

2016

English

375 Modelling and Understanding Pathomechanisms of X-Linked Recessive Ichthyosis in Vitro

Journal of Investigative Dermatology

English

X Linked Recessive Thrombocytopenia.

Journal of Medical Genetics

Genetics

1993

English

A New Chromosome X Exon-Specific Microarray Platform for Screening of Patients With X-Linked Disorders

Journal of Molecular Diagnostics

English

A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome

American Journal of Human Genetics

Genetics

1997

English

X‐linked Ichthyosis: Molecular Findings in Four Pedigrees With Inconspicuous Clinical Manifestations

Journal of Clinical Laboratory Analysis

Medical Laboratory Technology

Clinical Biochemistry

English

Expression of GPC3, an X-Linked Recessive Overgrowth Gene, Is Silenced in Malignant Mesothelioma

English

A Coinheritance of X-Linked and Autosomal Dominant Forms of the Ichthyosis

Biomedical Journal of Scientific & Technical Research

2019

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by R. E. Oakey

Cloning of a cDNA for Steroid Sulfatase: Frequent Occurrence of Gene Deletions in Patients With Recessive X Chromosome-Linked Ichthyosis.

Related publications

Increased Prevalence of Filaggrin Deficiency in 51 Patients With Recessive X-Linked Ichthyosis Presenting for Dermatological Examination

Comparing Histopathology From Patients With X-Linked Recessive Ichthyosis and Autosomal Recessive Congenital Ichthyosis With Transglutaminase 1 Mutation: A Report From the National Registry for Ichthyosis and Related Skin Disorders

375 Modelling and Understanding Pathomechanisms of X-Linked Recessive Ichthyosis in Vitro

X Linked Recessive Thrombocytopenia.

A New Chromosome X Exon-Specific Microarray Platform for Screening of Patients With X-Linked Disorders

A Gene for X-Linked Optic Atrophy Is Closely Linked to the Xp11.4-Xp11.2 Region of the X Chromosome

X‐linked Ichthyosis: Molecular Findings in Four Pedigrees With Inconspicuous Clinical Manifestations

Expression of GPC3, an X-Linked Recessive Overgrowth Gene, Is Silenced in Malignant Mesothelioma

A Coinheritance of X-Linked and Autosomal Dominant Forms of the Ichthyosis