Molecular cloning, characterization and 3D modelling of spotted snakehead fbn1 C-terminal region encoding asprosin and expression analysis of fbn1 | Scientific Reports
Parental mosaicism in Marfan and Ehlers–Danlos syndromes and related disorders | European Journal of Human Genetics
Localization of mutations in FBN1 and results from qualitative analysis... | Download Scientific Diagram
Characterization of MFS and MFSiPS cells. (A) DNA sequencing analysis... | Download Scientific Diagram
Marfan syndrome in the third Millennium | European Journal of Human Genetics
Recapitulating and Correcting Marfan Syndrome in a Cellular Model
An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to disease | Journal of Human Genetics
Position of polymorphic markers within and flanking the FBN1 gene (12) | Download Scientific Diagram
CRISPR/Cas9 in zebrafish: An attractive model for FBN1 genetic defects in humans - Yin - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
A New Mouse Model for Marfan Syndrome Presents Phenotypic Variability Associated with the Genetic Background and Overall Levels of Fbn1 Expression | PLOS ONE
Selection of marker RCGY sites and corresponding hybrid primers for... | Download Scientific Diagram
A Novel Heterozygous Intronic Mutation in the FBN1 Gene Contributes to FBN1 RNA Missplicing Events in the Marfan Syndrome
The Molecular Genetics of Marfan Syndrome
Solved You have obtained a human pedigree showing the | Chegg.com
Position of polymorphic markers within and flanking the FBN1 gene (12) | Download Scientific Diagram
Co-expression of FBN1 with mesenchyme-specific genes in mouse cell lines: implications for phenotypic variability in Marfan syndrome | European Journal of Human Genetics
Genes | Free Full-Text | Characterization of Two Novel Intronic Variants Affecting Splicing in FBN1-Related Disorders
Genes | Free Full-Text | FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review
Distribution of FBN1 mutations per module.The number of splice... | Download Scientific Diagram
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1 | Nature Genetics
Genes | Free Full-Text | Characterization of Two Novel Intronic Variants Affecting Splicing in FBN1-Related Disorders
Biomolecules | Free Full-Text | Fibrillin-1 Regulates Arteriole Integrity in the Retina
FBN1 gDNA Primers and Annealing Temperatures | Download Table
DNA Diagnostics of the Marfan Syndrome: Application of Amplifiable Polymorphic Markers | European Journal of Human Genetics
![Family-based whole-exome sequencing identifies novel loss-of-function mutations of FBN1 for Marfan syndrome [PeerJ]](https://dfzljdn9uc3pi.cloudfront.net/2018/5927/1/fig-1-full.png "Family-based whole-exome sequencing identifies novel loss-of-function mutations of FBN1 for Marfan syndrome [PeerJ]")
Family-based whole-exome sequencing identifies novel loss-of-function mutations of FBN1 for Marfan syndrome [PeerJ]
