1. Treatment With Methotrexate Associated With Lipid Core Nanoparticles Prevents Aortic Dilation in a Murine Model of Marfan Syndrome
   Maria Carolina Guido et al, 2022, Frontiers in Cardiovascular Medicine CrossRef
2. Genomic Applications in Inherited Genetic Disorders
   Bryan L. Krock et al, 2019, Genomic Applications in Pathology CrossRef
3. Genetic Factors of Comorbidity of Pelvic Organ Prolapse, Stress Urinary Incontinence, and Chronic Venous Insufficiency of the Lower Limbs in Women
   M. B. Khadzhieva et al, 2018, Russian Journal of Genetics CrossRef
4. A Giant Abdominal Aortic Aneurysm Revealing a Marfan Syndrome With a New FBN1 Mutation
   Laura Filippetti et al, 2021, Canadian Journal of Cardiology CrossRef
5. Detection of ten novel FBN1 mutations in Chinese patients with typical or incomplete Marfan syndrome and an overview of the genotype-phenotype correlations
   Linggen Gao et al, 2019, International Journal of Cardiology CrossRef
6. Affected-embryo-based SNP haplotyping with NGS for the preimplantation genetic testing of Marfan syndrome
   Yu Deng et al, 2021, Systems Biology in Reproductive Medicine CrossRef
7. Research Progress of Suspensory Ligaments of Lens
   若武 刘, 2023, Advances in Clinical Medicine CrossRef
8. Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese families
   Bo Gong et al, 2019, Molecular Genetics & Genomic Medicine CrossRef
9. Spontaneously Ruptured Dural Ectasia in a Patient with Marfan Syndrome: a Case Report and Discussion of the Challenges Faced
   Ifigeneia Gioti et al, 2021, SN Comprehensive Clinical Medicine CrossRef
10. Two Novel Pathogenic FBN1 Variations and Their Phenotypic Relationship of Marfan Syndrome
    Sinem Yalcintepe et al, 2020, Global Medical Genetics CrossRef
11. Selection of both habitat and genes in specialized and endangered caribou
    Maria Cavedon et al, 2022, Conservation Biology CrossRef
12. An integration into the diagnostic workflow in a pediatric patient suspected of having Marfan syndrome
    Maria Oro et al, 2022, Egyptian Journal of Medical Human Genetics CrossRef
13. Exome Sequencing Identifies a Novel FBN1 Variant in a Pakistani Family with Marfan Syndrome That Includes Left Ventricle Diastolic Dysfunction
    Nadia Farooqi et al, 2021, Genes CrossRef