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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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S Adamo

Showing results (71-80 of 76) with videos related to

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Science (New York, N.Y.)|October 29, 2011

Climate change. Preparing for resettlement associated with climate changeA de Sherbinin, M Castro, F Gemenne, et al.

Drugs|April 9, 2016

Erratum to: What to Do, and What Not to Do, When Diagnosing and Treating Breakthrough Cancer Pain (BTcP): Expert Opinion, R Vellucci, G Fanelli, et al.

Drugs|January 13, 2016

What to Do, and What Not to Do, When Diagnosing and Treating Breakthrough Cancer Pain (BTcP): Expert Opinion, R Vellucci, G Fanelli, et al.

American Journal of Human Genetics|December 3, 2021

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.

American Journal of Human Genetics|May 15, 2021

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.

American Journal of Human Genetics|November 9, 2022

EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesisChristin S Adamo, Aude Beyens, Alvise Schiavinato, et al.

Pageof 8

Search research articles

Showing results (71-80 of 76) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 76 results.

Science (New York, N.Y.)|October 29, 2011

Climate change. Preparing for resettlement associated with climate changeA de Sherbinin, M Castro, F Gemenne, et al.

Drugs|April 9, 2016

Erratum to: What to Do, and What Not to Do, When Diagnosing and Treating Breakthrough Cancer Pain (BTcP): Expert Opinion, R Vellucci, G Fanelli, et al.

Drugs|January 13, 2016

What to Do, and What Not to Do, When Diagnosing and Treating Breakthrough Cancer Pain (BTcP): Expert Opinion, R Vellucci, G Fanelli, et al.

American Journal of Human Genetics|December 3, 2021

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.

American Journal of Human Genetics|May 15, 2021

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.

American Journal of Human Genetics|November 9, 2022

EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesisChristin S Adamo, Aude Beyens, Alvise Schiavinato, et al.

Pageof 8