části přičítat rovnost fnb1 dna marker zmizet Běh fazole
Representative chromatogram of FBN1 sequence. (A) FBN1 has different... | 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
An iPSC-derived vascular model of Marfan syndrome identifies key mediators of smooth muscle cell death | Nature Genetics
A New Mouse Model for Marfan Syndrome Presents Phenotypic Variability Associated with the Genetic Background and Overall Levels of Fbn1 Expression | PLOS ONE
A positively selected FBN1 missense variant reduces height in Peruvian individuals | Nature
Fibrillins 1 and 2 Perform Partially Overlapping Functions during Aortic Development - ScienceDirect
A Novel Heterozygous Intronic Mutation in the FBN1 Gene Contributes to FBN1 RNA Missplicing Events in the Marfan Syndrome
Frontiers | Classification and Interpretation for 11 FBN1 Variants Responsible for Marfan Syndrome and Pre-implantation Genetic Testing (PGT) for Two Families Successfully Blocked Transmission of the Pathogenic Mutations
Biomolecules | Free Full-Text | Fibrillin-1 Regulates Arteriole Integrity in the Retina
Selection of marker RCGY sites and corresponding hybrid primers for... | Download Scientific Diagram
Parental mosaicism in Marfan and Ehlers–Danlos syndromes and related disorders | European Journal of Human Genetics
DNA methylation of 10 candidate biomarkers. a DNA methylation levels,... | Download Scientific Diagram
Family-based whole-exome sequencing identifies novel loss-of-function mutations of FBN1 for Marfan syndrome [PeerJ]
FBN1 mutation identification yield from different studies of Marfan and... | Download Table
Genes | Free Full-Text | FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review
Genes | Free Full-Text | Characterization of Two Novel Intronic Variants Affecting Splicing in FBN1-Related Disorders
Generation of Marfan patient specific iPSCs (ICSSUi001-A) carrying a novel heterozygous mutation in FBN1 gene - ScienceDirect
Position of polymorphic markers within and flanking the FBN1 gene (12) | Download Scientific Diagram
The Molecular Genetics of Marfan Syndrome
Genes | Free Full-Text | FBN1 Splice-Altering Mutations in Marfan Syndrome: A Case Report and Literature Review
CRISPR/Cas9 in zebrafish: An attractive model for FBN1 genetic defects in humans - Yin - 2021 - Molecular Genetics & Genomic Medicine - Wiley Online Library
An FBN1 pseudoexon mutation in a patient with Marfan syndrome: confirmation of cryptic mutations leading to disease | Journal of Human Genetics
Localization of mutations in FBN1 and results from qualitative analysis... | Download Scientific Diagram