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1 Ergebnisse
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DataSheet1_Epidermolysis Bullosa With Congenital Absence of..:
Pharuhad Pongmee
;
Sanchawan Wittayakornrerk
;
Ramrada Lekwuttikarn
...
doi:10.3389/fgene.2022.847150.s001. , 2022
Link:
https://doi.org/10.3389/fgene.2022.847150.s001
RT Journal T1
DataSheet1_Epidermolysis Bullosa With Congenital Absence of Skin: Congenital Corneal Cloudiness and Esophagogastric Obstruction Including Extended Genotypic Spectrum of PLEC, LAMC2, ITGB4 and COL7A1.docx
UL https://suche.suub.uni-bremen.de/peid=base-ftfrontimediafig:oai:figshare.com:article_19492865&Exemplar=1&LAN=DE A1 Pharuhad Pongmee A1 Sanchawan Wittayakornrerk A1 Ramrada Lekwuttikarn A1 Sasikarn Pakdeeto A1 Piangor Watcharakuldilok A1 Chatchay Prempunpong A1 Thipwimol Tim-Aroon A1 Chawintee Puttanapitak A1 Piyawan Wattanasoontornsakul A1 Thitiporn Junhasavasdikul A1 Parith Wongkittichote A1 Saisuda Noojarern A1 Duangrurdee Wattanasirichaigoon 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 bilateral hydronephrosis K1 cloudy cornea K1 epidermolysis bullosa with pyloric atresia K1 intestinal obstruction K1 reflux nephropathy JF doi:10.3389/fgene.2022.847150.s001 LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.847150.s001 DO https://doi.org/10.3389/fgene.2022.847150.s001 SF ELIB - SuUB Bremen
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