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Table_1_Case Report: Exome Sequencing Identified a Novel Co..:

Jing Zhang (23775) ; Huaying Hu (6569441) ; Weihong Mu (10147811)...
https://figshare.com/articles/dataset/Table_1_Case_Report_Exome_Sequencing_Identified_a_Novel_Compound_Heterozygous_Variation_in_PLOD2_Causing_Bruck_Syndrome_Type_2_DOC/14038199. , 2021

Link: https://doi.org/10.3389/fgene.2021.619948.s003

RT Journal
T1 <Title>Table_1_Case Report: Exome Sequencing Identified a Novel Compound Heterozygous Variation in PLOD2 Causing Bruck Syndrome Type 2.DOC</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_14038199&Exemplar=1&LAN=DE
				
A1 Jing Zhang (23775)
A1 Huaying Hu (6569441)
A1 Weihong Mu (10147811)
A1 Mei Yu (48172)
A1 Wenqi Chen (790608)
A1 Dongqing Mi (10147814)
A1 Kai Yang (73590)
A1 Qing Guo (317746)
YR 2021
K1 Genetics
K1 Genetic Engineering
K1 Biomarkers
K1 Developmental Genetics (incl. Sex Determination)
K1 Epigenetics (incl. Genome Methylation and Epigenomics)
K1 Gene Expression (incl. Microarray and other genome-wide approaches)
K1 Genome Structure and Regulation
K1 Genomics
K1 Genetically Modified Animals
K1 Livestock Cloning
K1 Gene and Molecular Therapy
K1 PLOD2 gene
K1 Bruck syndrome type 2
K1 osteogenesis imperfecta
K1 whole-exome sequencing
K1 immunohistochemistry detection
JF https://figshare.com/articles/dataset/Table_1_Case_Report_Exome_Sequencing_Identified_a_Novel_Compound_Heterozygous_Variation_in_PLOD2_Causing_Bruck_Syndrome_Type_2_DOC/14038199
LK http://dx.doi.org/https://doi.org/10.3389/fgene.2021.619948.s003
DO https://doi.org/10.3389/fgene.2021.619948.s003
SF ELIB - SuUB Bremen

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