Y. Pan

Molecular evidence that the p55 gene is not responsible for either of two Xq28-linked disorders: Emery-Dreifuss muscular dystrophy and dyskeratosis congenita.

J. Gitschier, S. Das, G. Pai, 1994, American journal of human genetics.

Translocation breakpoints of chromosome 4 in male carriers: clinical features and implications for genetic counseling.

R. Wang, X. Yang, R. Z. Liu, 2016, Genetics and molecular research : GMR.

Translocation breakpoints of chromosome 1 in male carriers: clinical features and implications for genetic counseling.

F. Yue, R. Wang, D. Zhu, 2016, Genetics and molecular research : GMR.

Chromosome 7 translocation breakpoints in male carriers: clinical features and implications for genetic counseling.

F. Yue, R. Wang, R. Z. Liu, 2016, Genetics and molecular research : GMR.

Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia.

Z. Zhang, Y. Dong, R. Liu, 2015, Genetics and molecular research : GMR.

Two novel DAX1 gene mutations in Chinese patients with X-linked adrenal hypoplasia congenita: Clinical, hormonal and genetic analysis

X. Wu, L. Ni, L. Ruan, 2011, Journal of Endocrinological Investigation.

The effect of eight V2 vasopressin receptor mutations on stimulation of adenylyl cyclase and binding to vasopressin.

P. Wilson, J. Gitschier, Y. Pan, 1994, The Journal of biological chemistry.