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Table2_Whole Exome Sequencing Identified Novel ARMC9 Variat..:
Hao Wang (39217)
;
Guanjun Luo (12045092)
;
Wensheng Hu (9107163)
...
https://figshare.com/articles/dataset/Table2_Whole_Exome_Sequencing_Identified_Novel_ARMC9_Variations_in_Two_Cases_With_Joubert_Syndrome_docx/19121354. , 2022
Link:
https://doi.org/10.3389/fgene.2022.817153.s002
RT Journal T1
Table2_Whole Exome Sequencing Identified Novel ARMC9 Variations in Two Cases With Joubert Syndrome.docx
UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_19121354&Exemplar=1&LAN=DE A1 Hao Wang (39217) A1 Guanjun Luo (12045092) A1 Wensheng Hu (9107163) A1 Jin Mei (12045095) A1 Yue Shen (132970) A1 Min Wang (21070) A1 Yuan Tan (819132) A1 Yang Yang (45629) A1 Chao Lu (4374) A1 Yong Zhao (84950) A1 Ming Qi (191355) YR 2022 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 Joubert syndrome K1 ARMC9 gene K1 whole-exome sequencing K1 molecular dynamic analysis K1 minigene system JF https://figshare.com/articles/dataset/Table2_Whole_Exome_Sequencing_Identified_Novel_ARMC9_Variations_in_Two_Cases_With_Joubert_Syndrome_docx/19121354 LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.817153.s002 DO https://doi.org/10.3389/fgene.2022.817153.s002 SF ELIB - SuUB Bremen
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