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Baitao Zeng

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Frontiers in Behavioral Neuroscience|November 29, 2023

Identification of five novel <i>SCN1A</i> variantsBaitao Zeng, Haoyi Zhang, Qing Lu, et al.

Scientific Reports|April 25, 2025

Clinical experience of the expanded carrier screening for recessive genetic diseases in a large cohort study in Southern central ChinaLu Pan, Haiyan Luo, Tingting Huang, et al.

Cancer Cell International|February 5, 2020

Mesenchymal stem cells derived from iPSCs expressing interleukin-24 inhibit the growth of melanoma in the tumor-bearing mouse modelZheng Wu, Wei Liu, Zujia Wang, et al.

Orphanet Journal of Rare Diseases|August 22, 2024

Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center studyQing Lu, Laipeng Luo, Baitao Zeng, et al.

Human Molecular Genetics|April 27, 2024

Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNAYan Yang, Haiyan Luo, Lijuan Pan, et al.

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Search research articles

Showing results (11-20 of 15) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 15 results.

Frontiers in Behavioral Neuroscience|November 29, 2023

Identification of five novel <i>SCN1A</i> variantsBaitao Zeng, Haoyi Zhang, Qing Lu, et al.

Scientific Reports|April 25, 2025

Clinical experience of the expanded carrier screening for recessive genetic diseases in a large cohort study in Southern central ChinaLu Pan, Haiyan Luo, Tingting Huang, et al.

Cancer Cell International|February 5, 2020

Mesenchymal stem cells derived from iPSCs expressing interleukin-24 inhibit the growth of melanoma in the tumor-bearing mouse modelZheng Wu, Wei Liu, Zujia Wang, et al.

Orphanet Journal of Rare Diseases|August 22, 2024

Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center studyQing Lu, Laipeng Luo, Baitao Zeng, et al.

Human Molecular Genetics|April 27, 2024

Reevaluating the splice-altering variant in TECTA as a cause of nonsyndromic hearing loss DFNA8/12 by functional analysis of RNAYan Yang, Haiyan Luo, Lijuan Pan, et al.

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