Qizong Lao

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 4

Top Topics

Peritoneal Dialysis

Single Molecule

Top Venues

Molecular genetics & genomic medicine

European journal of human genetics : EJHG

The Journal of clinical endocrinology and metabolism

This page only lists publications with an associated author ORCID identifier.

Publications

Qizong Lao, Deepika D'Cunha Burkardt, Sarah Kollender, Fabio Rueda Faucz, Deborah P Merke
Congenital adrenal hyperplasia due to two rare CYP21A2 variant alleles, including a novel attenuated CYP21A1P/CYP21A2 chimera. Molecular genetics & genomic medicine (2023)
Qizong Lao, Deborah P Merke
Letter to the Editor from Lao and Merke: "Ehlers-Danlos Syndrome: Molecular and Clirnical Characterization of TNXA/TNXB Chimeras in Congenital Adrenal Hyperplasia". The Journal of clinical endocrinology and metabolism 106 (7) (2021)
Qizong Lao, Deborah P Merke
Molecular genetic testing of congenital adrenal hyperplasia due to 21-hydroxylase deficiency should include CAH-X chimeras. European journal of human genetics : EJHG 29 (7) (2021)
Qizong Lao, Ashwini Mallappa, Fabio Rueda Faucz, Elizabeth Joyal, Padmasree Veeraraghavan, Wuyan Chen, Deborah P Merke
A TNXB splice donor site variant as a cause of hypermobility type Ehlers-Danlos syndrome in patients with congenital adrenal hyperplasia. Molecular genetics & genomic medicine 9 (2) (2020)