Aizhen Yan

Identification of two de novo mutations in Chinese patients with X-linked adrenoleukodystrophy

F. Lan, Long-feng Ke, Zhihong Wang, 2008, Clinical chemistry and laboratory medicine.

Alternatively spliced products lacking exon 12 dominate the expression of fragile X mental retardation 1 gene in human tissues.

J. Liao, F. Lan, Xian-Guo Fu, 2015, Molecular medicine reports.

Familial Skewed X Chromosome Inactivation in Adrenoleukodystrophy Manifesting Heterozygotes from a Chinese Pedigree

F. Lan, Zhihong Wang, Hai-hua Xie, 2013, PloS one.

[Genetic diagnosis and analysis of related genes for a pedigree with 2p25 and 12p13 cryptic rearrangements].

Jian Zeng, Xiao Zhang, F. Lan, 2014, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Hybrid minigene splicing assay verified the pathogenicity of a novel splice site variant in the dystrophin gene of a Chinese patient with typical Duchenne muscular dystrophy phenotype

Jian Zeng, Yan-hong Lin, F. Lan, 2016, Clinical chemistry and laboratory medicine.

Establishment of a molecular diagnostic system for spinal muscular atrophy experience from a clinical laboratory in china.

Jian Zeng, Yan-hong Lin, F. Lan, 2011, The Journal of molecular diagnostics : JMD.

Whole-exome sequencing identifies compound heterozygous mutations in ARSA of two siblings presented with atypical onset of metachromatic leukodystrophy from a Chinese pedigree.

Yan-hong Lin, F. Lan, Zhihong Wang, 2016, Clinica chimica acta; international journal of clinical chemistry.

Alternatively spliced products lacking exon 12 dominate the expression of fragile X mental retardation 1 gene in human tissues.

J. Liao, F. Lan, Xian-Guo Fu, 2015, Molecular medicine reports.