Hong-wei Ma

发表

Novel compound heterozygous variants in the TAF6 gene in a patient with Alazami-Yuan syndrome: A case report

Shuang-Zhu Lin, Jingqi Feng, Li-ping Sun, 2022, World journal of clinical cases.

Schinzel–Giedion syndrome: a novel case, review and revised diagnostic criteria

Zhi-Xu He, Wei-Liang Liu, Fang Li, 2018, Journal of Genetics.

Primary Intracranial Leiomyosarcoma: Review of the Literature and Presentation of a Case

Gangge Cheng, Yan Zhou, Hong-wei Ma, 2012, Oncology Research and Treatment.

PTEN gene and AKT/mTOR pathway in gynecological cancers and cancer immune escape

M. Xi, Hong-wei Ma, Xi Zeng, 2022, European Journal of Gynaecological Oncology.

Possible genetic heterogeneity in the Saethre-Chotzen syndrome

A. Munnich, D. Rénier, M. Merrer, 1996, Human Genetics.

FGFR2 mutations in Pfeiffer syndrome

A. Munnich, J. Bonaventure, D. Rénier, 1995, Nature Genetics.

CNTNAP2 Is Significantly Associated With Speech Sound Disorder in the Chinese Han Population

Hong-wei Ma, Yun-jing Zhao, Yue-Ping Wang, 2015, Journal of child neurology.

[Value of integrated visual and auditory continuous performance test in the diagnosis of childhood attention deficit hyperactivity disorder].

Hong-wei Ma, Xiao-mei Dai, Xue-xia Pan, 2007, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Schinzel–Giedion syndrome: a novel case, review and revised diagnostic criteria

Wei-Liang Liu, Fang Li, R. Ai, 2018, Journal of Genetics.

MeCP2 gene mutation analysis in autistic boys with developmental regression

Yao Lu, Hong-wei Ma, Yun-jing Zhao, 2007, Psychiatric genetics.

Association between FOXP2 gene and speech sound disorder in Chinese population

Hong-wei Ma, Guangrong Qiu, Yun-jing Zhao, 2010, Psychiatry and clinical neurosciences.

[Comparative study on sensory integration function in children with primary nocturnal enuresis].

Hong-wei Ma, Fang Liu, Xiao-bo Tian, 2010, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

[Relationship between dopamine D4 receptor gene polymorphisms and primary nocturnal enuresis].

Yao Lu, Hong-wei Ma, Xiao-mei Dai, 2008, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

[Clinical features and C12orf65 mutations of autosomal recessive spastic paraplegia-55: a case report].

Hong-wei Ma, Xian-Ting Sun, Shuangzhu Lin, 2019, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

[Gene mutation analysis in patients with propionic acidemia].

X. Gu, Li Liu, Yanling Yang, 2008, Zhonghua er ke za zhi = Chinese journal of pediatrics.

[Relationship between gene mutations and intelligence in children with Duchenne muscular dystrophy].

Man Hu, Hong-wei Ma, Xiao-bo Tian, 2011, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China

Xiong-ying Yu, F. Luo, Xiao-hong Chen, 2022, Orphanet Journal of Rare Diseases.

[NIPBL gene mutations in two children with Cornelia de Lange syndrome].

Hong-wei Ma, Yun-jing Zhao, 2018, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

[Association analysis on the polymorphisms of PCOL2 and Sp1 binding sites of COL1A1 gene and the congenital dislocation of the hip in Chinese population].

Hong-wei Ma, Li-jun Zhang, Qiwi Li, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.