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Publications by Yibei Wang

TCOF1 Pathogenic Variants Identified by Whole-Exome Sequencing in Chinese Treacher Collins Syndrome Families and Hearing Rehabilitation Effect

Orphanet Journal of Rare Diseases

English

Related publications

Identification of a Novel TCOF1 Mutation in a Chinese Family With Treacher Collins Syndrome

Experimental and Therapeutic Medicine

Cancer Research

English

Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing

Hormone Research in Paediatrics

English

Mutation in Exon 13 of the TCOF1 Gene in Patient With Treacher Collins Syndrome

Acta Fytotechnica et Zootechnica

English

Treacher-Collins Syndrome

English

Identification of CDH23 Mutations in Korean Families With Hearing Loss by Whole-Exome Sequencing

BMC Medical Genetics

English

Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families

Multidisciplinary

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

Reproductive Medicine

English

Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants

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

Multidisciplinary

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Whole-Exome Sequencing Analysis of Waardenburg Syndrome in a Chinese Family

Human Genome Variation

Molecular Biology

English