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Publications by Zhengfeng Xu

Identification of Two Novel LAMA2 Mutations in a Chinese Patient With Congenital Muscular Dystrophy

Frontiers in Genetics
GeneticsMolecular Medicine
2018English

A Single Cell Level Based Method for Copy Number Variation Analysis by Low Coverage Massively Parallel Sequencing

PLoS ONE
Multidisciplinary
2013English

Analyzing False‐negative Results Detected in Low‐risk Non‐invasive Prenatal Screening Cases

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2020English

A De Novo Heterozygous Frameshift Mutation Identified in BCL11B Causes Neurodevelopmental Disorder by Whole Exome Sequencing

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

Identification and Characterization of a Novel 43-Bp Deletion Mutation of the ATP7B Gene in a Chinese Patient With Wilson’s Disease: A Case Report

BMC Medical Genetics
Genetics
2018English

Molecular Characterization of Ring Chromosome 18 by Low-Coverage Next Generation Sequencing

BMC Medical Genetics
Genetics
2015English

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