Hai-rong Wu

发表

Chromosome Xq28 duplication encompassing MECP2: Clinical and molecular analysis of 16 new patients from 10 families in China.

Y. Qi, Z. Yi, H. Pan, 2016, European journal of medical genetics.

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

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

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.

Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies.

Y. Qi, L. Zou, D. Bu, 2010, Mitochondrion.

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.

Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization

Y. Qi, X. Bao, H. Pan, 2016, Chinese medical journal.

Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome.

Y. Qi, H. Pan, Lin Li, 2016, Taiwanese journal of obstetrics & gynecology.

Array CGH-based Detection and Characterization of Combined 1p36 Deletion and 22q13 Duplication in a Boy and a Fetus from a Single Family

Y. Qi, Z. Yi, H. Pan, 2017 .

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.