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Table2_Prenatal phenotype analysis and mutation identificat..:
Laura Moreno-Leon
;
Marco A. Quezada-Ramirez
;
Evan Bilsbury
...
doi:10.3389/fgene.2022.982127.s004. , 2022
Link:
https://doi.org/10.3389/fgene.2022.982127.s004
RT Journal T1
Table2_Prenatal phenotype analysis and mutation identification of a fetus with meckel gruber syndrome.pdf
UL https://suche.suub.uni-bremen.de/peid=base-ftfrontimediafig:oai:figshare.com:article_20515284&Exemplar=1&LAN=DE A1 Laura Moreno-Leon A1 Marco A. Quezada-Ramirez A1 Evan Bilsbury A1 Courtney Kiss A1 Andrea Guerin A1 Hemant Khanna 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 cilia K1 ciliopathies K1 RPGRIP1L K1 meckel-gruber syndrome K1 ciliary defects JF doi:10.3389/fgene.2022.982127.s004 LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.982127.s004 DO https://doi.org/10.3389/fgene.2022.982127.s004 SF ELIB - SuUB Bremen
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