M. Ma

发表

TARDBP gene mutations among Chinese patients with sporadic amyotrophic lateral sclerosis

Rui Huang, H. Shang, Xiaoyan Guo, 2012, Neurobiology of Aging.

A novel missense mutation in GTP cyclohydrolase I (GCH1) gene causes dopa‐responsive dystonia in Chinese Han population

F. Hu, D. Zhou, M. Ma, 2011, European journal of neurology.

GCH1 mutation and clinical study of Chinese patients with dopa‐responsive dystonia

H. Shang, Yuan Yang, Xiaoyan Guo, 2010, Movement disorders : official journal of the Movement Disorder Society.

Differential effect of specific gr/gr deletion subtypes on spermatogenesis in the Chinese Han population.

L. Li, D. Tao, D. Su, 2010, International journal of andrology.

Phenotypic expression of partial AZFc deletions is independent of the variations in DAZL and BOULE in a Han population.

D. Tao, Yongxin Ma, Yunqiang Liu, 2010, Journal of andrology.

Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment.

D. Tao, Yongxin Ma, Yunqiang Liu, 2008, Human reproduction.

Massive deletion in AZFb/b+c and azoospermia with Sertoli cell only and/or maturation arrest.

Y. Yang, L. Li, M. Ma, 2008, International journal of andrology.

Evidence for the association of Y-chromosome haplogroups with susceptibility to spermatogenic failure in a Chinese Han population

L. Li, D. Tao, Y. Liu, 2007, Journal of Medical Genetics.

Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease

Lin Zou, Yongxin Ma, Yunqiang Liu, 2011, BMC Medical Genetics.

Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population

H. Shang, D. Tao, Yongxin Ma, 2010, Journal of the Neurological Sciences.

The c.323 G>C mutation in LORICRIN causes new-found late-onset autosomal dominant loricrin keratoderma in a Chinese Han Pedigree.

Jingyan Yi, Yongmei Liao, Jiao Zhao, 2022, Journal of dermatological science.

[Study on the distribution of Y chromosome haplogroups in Sichuan Han population].

Si-zhong Zhang, Yuan Yang, M. Ma, 2007, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Some single-nucleotide polymorphisms of the TSSK2 gene may be associated with human spermatogenesis impairment.

Yongxin Ma, Yunqiang Liu, D. Su, 2010, Journal of andrology.

GCH1 mutation and clinical study of Chinese patients with dopa‐responsive dystonia

H. Shang, Yuan Yang, Xiaoyan Guo, 2010, Movement disorders : official journal of the Movement Disorder Society.

Some single-nucleotide polymorphisms of the TSSK2 gene may be associated with human spermatogenesis impairment.

Yongxin Ma, Yunqiang Liu, D. Su, 2010, Journal of andrology.