Lin-bei Deng

发表

Prenatal diagnosis and outcome of fetal hyperechogenic kidneys in the era of antenatal next-generationsequencing.

Luming Sun, Yingjun Yang, Yong Liu, 2022, Clinica chimica acta; international journal of clinical chemistry.

A clear bias in parental origin of de novo pathogenic CNVs related to intellectual disability, developmental delay and multiple congenital anomalies

Jing Guo, Desheng Liang, Lingqian Wu, 2017, Scientific Reports.

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.

D. Liang, D. Cram, Lingqian Wu, 2014, The Journal of molecular diagnostics : JMD.

Chromosomal abnormalities in recurrent pregnancy loss and its association with clinical characteristics

Luming Sun, G. Zou, Xing Wei, 2023, Journal of Assisted Reproduction and Genetics.

Prenatal diagnosis of Wolf–Hirschhorn syndrome: from ultrasound findings, diagnostic technology to genetic counseling

S. Cheung, Yong Liu, J. Holder, 2018, Archives of Gynecology and Obstetrics.

Value of Exome Sequencing in Diagnosis and Management of Recurrent Non-immune Hydrops Fetalis: A Retrospective Analysis

Yaping Yang, Jian Wang, Xietong Wang, 2021, Frontiers in Genetics.

Brief report. Adult patient presenting an interstitial (9) (q21.32q31.1) direct duplication resulting from the malsegregation of a paternal balanced insertional translocation.

D. Liang, Lingqian Wu, Jing Liu, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Prenatal diagnosis of skeletal dysplasias using a targeted skeletal gene panel

Luming Sun, N. Chandler, Xinyao Zhou, 2018, Prenatal diagnosis.

Targeted gene panel sequencing prenatally detects two novel mutations of DYNC2H1 in a fetus with increased biparietal diameter and polyhydramnios.

S. Cheung, E. Schmitt, Luming Sun, 2018, Birth defects research.

Intrauterine phenotype features of fetuses with Williams–Beuren syndrome and literature review

Luming Sun, Yingjun Yang, Linbei Deng, 2019, Annals of human genetics.