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3. Clinical Impact of Copy Number Variation on the Genetic Diagnosis of Syndromic Aortopathies. (30th July 2021)

4. Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene. Issue 2 (9th February 2022)

7. Impact of pathogenic FBN1 variant types on the development of severe scoliosis in patients with Marfan syndrome. Issue 1 (16th December 2021)

8. Impact of Pathogenic FBN1 Variant Types on the Progression of Aortic Disease in Patients With Marfan Syndrome. (June 2018)

9. Long-Term renal function after implantation of continuous-flow left ventricular assist devices: A single center study. (December 2021)

10. Nonsyndromic arteriopathy and aortopathy and vascular Ehlers–Danlos syndrome causing COL3A1 variants. Issue 9 (11th May 2022)