Xue-fei Zheng

Mitochondrial DNA Copy Number in Rett Syndrome Caused by MECP2 Variants.

Y. Qi, X. Bao, H. Pan, 2021, The Journal of pediatrics.

Deletion of a 4977-bp Fragment in the Mitochondrial Genome Is Associated with Mitochondrial Disease Severity

Y. Qi, Sai-nan Zhu, D. Bu, 2015, PloS one.

Wild-Type Mitochondrial DNA Copy Number in Urinary Cells as a Useful Marker for Diagnosing Severity of the Mitochondrial Diseases

Y. Qi, Sai-nan Zhu, L. Zou, 2013, PloS one.

Molecular diagnosis of Phenylketonuria in 157 Families and Prenatal Diagnosis of Phenylketonuria

H. Pan, Qiang Gu, Hai-rong Wu, 2019 .

Genetic analysis and prenatal diagnosis of 76 Chinese families with X‐linked adrenoleukodystrophy

Y. Qi, Siwen Liu, X. Bao, 2021, Molecular genetics & genomic medicine.

Molecular diagnosis of phenylketonuria in 157 Chinese families and the results of prenatal diagnosis in these families

H. Pan, Qiang Gu, Hai-rong Wu, 2021, Chinese medical journal.

[Screening of mitochondrial deoxyribonucleic acid 3271T > C, 8356T > C, 9176T > C/G and 13513G > A mutations in mitochondrial encephalomyopathies].

Y. Qi, D. Bu, H. Pan, 2011, Zhonghua yi xue za zhi.