Hong-yong Lu

A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenesis imperfecta type II.

Xiaojun Li, Hao-yang Wang, Yanning Hou, 2009, Mutation research.

A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21–12p12.2 by oligonucleotide array CGH

Hong-yong Lu, Yu-feng Huang, B. Yao, 2009, American journal of medical genetics. Part A.

A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family.

Yi Shi, Bin-Cheng Yang, Hao-yang Wang, 2008, Clinica chimica acta; international journal of clinical chemistry.

ORIGINAL ARTICLE: A rare Y chromosome constitutional rearrangement: a partial AZFb deletion and duplication within chromosome Yp in an infertile man with severe oligoasthenoteratozoospermia: Partial AZFb deletion and duplication within Yp

Hao-yang Wang, Hong-yong Lu, Yu-feng Huang, 2010 .

A case of agonadism associated with y-chromosome rearrangement: cytogenetic and molecular studies.

Li Jia, Hong-yong Lu, Hai-feng Shao, 2009, Journal of andrology.

Rapid molecular prenatal diagnosis of spondyloepiphyseal dysplasia congenita by PCR-SSP assay.

Hong-yong Lu, Yu-feng Huang, G. Zhou, 2008, Genetic testing.

[A girl with partial monosomy 18q21: cytogenetic and molecular genetics studies].

Hong-yong Lu, Yu-feng Huang, B. Yao, 2008, Yi chuan = Hereditas.

A rare Y chromosome constitutional rearrangement: a partial AZFb deletion and duplication within chromosome Yp in an infertile man with severe oligoasthenoteratozoospermia.

H. Y. Wang, Hao-yang Wang, Hong-yong Lu, 2011, International journal of andrology.