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Publications by Wenjin Yan

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

Molecular Medicine Reports
OncologyGeneticsMolecular BiologyBiochemistryCancer ResearchMolecular Medicine
2018English

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Schwartz Jampel Syndrome- A Case Report

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

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Two Novel NPHS1 Mutations in a Chinese Family With Congenital Nephrotic Syndrome

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2011English

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

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A Novel Mutation in the TG Gene (G2322S) Causing Congenital Hypothyroidism in a Sudanese Family: A Case Report

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Case Report: A Case of PAI-1 4g/5g Heterozygosity Causing Budd-Chiari Syndrome

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Waardenburg Syndrome Type 1: Case Report

The Journal of Kartal Training and Research Hospital
2014English

A Novel Dominant Mutation in the SOX10 Gene in a Chinese Family With Waardenburg Syndrome Type�II

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2019English

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

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2020English

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