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Publications by Guimei Zhou

Usher Syndrome Type III: Revised Genomic Structure of the USH3 Gene and Identification of Novel Mutations

American Journal of Human Genetics

Genetics

2002

English

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∩Revised Genomic Structure of the Human Ghrelin Gene and Identification of Novel Exons, Alternative Splice Variants and Natural Antisense Transcripts

English

Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

PLoS ONE

Multidisciplinary

2013

English

Identification of Novel ROR2 Gene Mutations in Indian Children With Robinow Syndrome

JCRPE Journal of Clinical Research in Pediatric Endocrinology

English

Gray Platelet Syndrome: Novel Mutations of the NBEAL2 Gene

American Journal of Hematology

Hematology

2017

English

Novel USH2A Mutations in Japanese Usher Syndrome Type 2 Patients: Marked Differences in the Mutation Spectrum Between the Japanese and Other Populations

Journal of Human Genetics

Genetics

2011

English

Origin of Vestibular Dysfunction in Usher Syndrome Type 1B

Neurobiology of Disease

Neurology

2001

English

Lentiviral Gene Replacement Therapy of Retinas in a Mouse Model for Usher Syndrome Type 1B

English

Identification of Novel and Recurrent Mutations in the Calcium Binding Type III Repeats of Cartilage Oligomeric Matrix Protein in Patients With Pseudoachondroplasia

Genetics and Molecular Research

English

Profound, Prelingual Nonsyndromic Deafness Maps to Chromosome 10q21 and Is Caused by a Novel Missense Mutation in the Usher Syndrome Type IF Gene PCDH15

European Journal of Human Genetics

Genetics

2009

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Guimei Zhou

Usher Syndrome Type III: Revised Genomic Structure of the USH3 Gene and Identification of Novel Mutations

Related publications

∩Revised Genomic Structure of the Human Ghrelin Gene and Identification of Novel Exons, Alternative Splice Variants and Natural Antisense Transcripts

Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

Identification of Novel ROR2 Gene Mutations in Indian Children With Robinow Syndrome

Gray Platelet Syndrome: Novel Mutations of the NBEAL2 Gene

Novel USH2A Mutations in Japanese Usher Syndrome Type 2 Patients: Marked Differences in the Mutation Spectrum Between the Japanese and Other Populations

Origin of Vestibular Dysfunction in Usher Syndrome Type 1B

Lentiviral Gene Replacement Therapy of Retinas in a Mouse Model for Usher Syndrome Type 1B

Identification of Novel and Recurrent Mutations in the Calcium Binding Type III Repeats of Cartilage Oligomeric Matrix Protein in Patients With Pseudoachondroplasia

Profound, Prelingual Nonsyndromic Deafness Maps to Chromosome 10q21 and Is Caused by a Novel Missense Mutation in the Usher Syndrome Type IF Gene PCDH15