M. Hou

Gene analysis: A rare gene disease of intellectual deficiency-Cohen syndrome

Wei Wei, Cheng-qing Yang, Zongbo Chen, 2018, International Journal of Developmental Neuroscience.

Chinese Cases of Metachromatic Leukodystrophy with the Novel Missense Mutations in ARSA Gene

L. Yi, Zongbo Chen, Jie Song, 2020, Journal of Molecular Neuroscience.

Association of Interleukin-6-572C/G Gene Polymorphism and Serum or Cerebrospinal Fluid Interleukin-6 Level with Enterovirus 71 Encephalitis in Chinese Han Patients with Hand, Foot, and Mouth Disease

Jian Li, Zongbo Chen, Pei-pei Liu, 2014, Inflammation.

Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report

Li-ping Chen, Zongbo Chen, Pei-pei Liu, 2018, BMC Medical Genetics.

Genetic Variation Analysis and Treatment Strategy of 20 Patients with Dystrophin Gene Mutations

Fei Li, Wei Wei, Cheng-qing Yang, 2020 .

Applicability of genetic polymorphism analysis for the diagnosis of Angelman syndrome and the correlation between language difficulties and disease phenotype.

M. Hou, K. Wang, Y. Li, 2016, Genetics and molecular research : GMR.

Four novel compound heterozygous mutations in C5orf42 gene in patients with pure and mild Joubert syndrome

Wei Wei, M. Hou, Dian-rong Sun, 2020, International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience.

Novel variants in TBC1D24 associated with epilepsy and deafness: Report of two cases

N. Zhang, Wei Wei, Zongbo Chen, 2020, International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience.

Clinical characteristics and functional status of children with different subtypes of dyskinetic cerebral palsy

M. Hou, Yu-tang Li, Dian-rong Sun, 2018, Medicine.

Levodopa is effective in the treatment of three Chinese Tyrosine hydroxylase (TH) deficiency children

Wei Wei, Cheng-qing Yang, Zongbo Chen, 2019, International Journal of Developmental Neuroscience.

Microcephaly, disproportionate pontine, and cerebellar hypoplasia syndrome: Two novel mutations in the CASK gene were discovered in Chinese females

Wei Wei, M. Hou, Dian-rong Sun, 2021, International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience.

Association of Interleukin-6-572C/G Gene Polymorphism and Serum or Cerebrospinal Fluid Interleukin-6 Level with Enterovirus 71 Encephalitis in Chinese Han Patients with Hand, Foot, and Mouth Disease

Zongbo Chen, Pei-pei Liu, M. Hou, 2015, Inflammation.