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Publications by Zhenqing Luo

Case Report: Two Novel VPS13B Mutations in a Chinese Family With Cohen Syndrome and Hyperlinear Palms

BMC Medical Genetics

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Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant With Autistic-Like Features

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Novel HSPG2 Mutations Causing Schwartz‑Jampel Syndrome Type 1 in a Chinese Family: A Case Report

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Novel Compound Heterozygous TMEM67 Variants in a Vietnamese Family With Joubert Syndrome: A Case Report

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Novel NPHS1 Splice Site Mutations in a Chinese Child With Congenital Nephrotic Syndrome

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Novel Mutations in COL4A3, COL4A4, and COL4A5 in Chinese Patients With Alport Syndrome

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A Novel TRPS1 Mutation in a Moroccan Family With Tricho-Rhino-Phalangeal Syndrome Type III: Case Report

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

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Identification of Two Novel LAMA2 Mutations in a Chinese Patient With Congenital Muscular Dystrophy

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