B. Tang

Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia

Zhening Liu, Haihong Liu, Jingping Zhao, 2016, Scientific Reports.

Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases

W. Reardon, R. Hennekam, H. Cavé, 2005, Journal of Medical Genetics.

Congenital ulcerating hemangioma in a baby with KRAS mutation and cardio-facio-cutaneous syndrome.

W. Reardon, B. Kerr, G. Black, 2007, Clinical dysmorphology.

Severe neonatal manifestations of Costello syndrome

B. Kerr, S. Lam, C. Brewer, 2007, Journal of Medical Genetics.

SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS

T. Hornemann, B. Tang, S. Zeng, 2022, medRxiv.