L. Gong

Inborn errors of metabolism detectable by tandem mass spectrometry in Beijing

Y. Kong, Wei Liu, N. Yang, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

Identification and molecular analysis of 11 cases of the PTS gene variants associated with tetrahydrobiopterin deficiency

Y. Kong, Yue Tang, N. Yang, 2022, Frontiers in Genetics.

Circular RNA circCTNNA1 promotes colorectal cancer progression by sponging miR-149-5p and regulating FOXM1 expression

A. Wu, L. Gong, Peng-ju Chen, 2020, Cell Death & Disease.

Identification of gene mutations in six Chinese patients with maple syrup urine disease

Y. Kong, T. Ji, N. Yang, 2023, Frontiers in Genetics.

A pilot study on newborn screening for congenital adrenal hyperplasia in Beijing

Y. Kong, N. Yang, L. Gong, 2019, Journal of Pediatric Endocrinology & Metabolism (JPEM).

Whole-exome sequencing as a powerful tool for identifying genetic causes in a patient with POLG-related disorders and phenylketonuria

C. Yin, Y. Kong, Chengrong Wang, 2019, The Journal of international medical research.

Clinical characteristics and genetics analysis for the ITD of congenital hypothyroidism

Y. Kong, N. Yang, L. Gong, 2022, Journal of pediatric endocrinology & metabolism : JPEM.