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. Human DNA Mutations and their Impact on Genetic Disorders
    Safia Samir, 2024, Recent Patents on Biotechnology CrossRef
  4. 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
  5. Contributions of Germline and Somatic Mosaic Genetics to Thoracic Aortic Aneurysms in Nonsyndromic Individuals
    Ming Hui Chen et al, 2024, Journal of the American Heart Association CrossRef
  6. A Giant Abdominal Aortic Aneurysm Revealing a Marfan Syndrome With a New FBN1 Mutation
    Laura Filippetti et al, 2021, Canadian Journal of Cardiology CrossRef
  7. 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
  8. 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
  9. Research Progress of Suspensory Ligaments of Lens
    若武 刘, 2023, Advances in Clinical Medicine CrossRef
  10. 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
  11. 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
  12. Two Novel Pathogenic FBN1 Variations and Their Phenotypic Relationship of Marfan Syndrome
    Sinem Yalcintepe et al, 2020, Global Medical Genetics CrossRef
  13. Selection of both habitat and genes in specialized and endangered caribou
    Maria Cavedon et al, 2022, Conservation Biology CrossRef
  14. 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
  15. 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
  16. Visual Outcomes in Ectopia Lentis in Marfan Syndrome: A Study of Four Surgical Techniques in Children and Adults
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