Lao, Qizong

High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia.

Lao, Q., Brookner, B., & Merke, D. P. (2019) · The Journal of Molecular Diagnostics

Sexual Differentiation and DisordersConnective tissue disorders research

Cited by 29

Complement component 4 variations may influence psychopathology risk in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Lao, Q., Jardin, M. D., Jayakrishnan, R., Ernst, M., & Merke, D. P. (2018) · Human Genetics

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 12

Congenital adrenal hyperplasia due to two rare CYP21A2 variant alleles, including a novel attenuated CYP21A1P/CYP21A2 chimera

Lao, Q., Burkardt, D. D., Kollender, S., Faucz, F. R., & Merke, D. P. (2023) · Molecular Genetics & Genomic Medicine

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 8

Pseudogene TNXA Variants May Interfere with the Genetic Testing of CAH-X

Lao, Q., Zhou, K., Parker, M., Faucz, F. R., & Merke, D. P. (2023) · Genes

Sexual Differentiation and DisordersConnective tissue disorders research

Cited by 1