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Early diagnosis of Werner's syndrome using exome-wide sequencing in a single, atypical patient.

journal contribution
posted on 2023-06-07, 20:37 authored by Eleanor Raffan, Liam A Hurst, Saeed Al Turki, Gillian Carpenter, Carol Scott, Allan Daly, Alison Coffey, Sanjeev Bhaskar, Eleanor Howard, Naz Khan, Helen Kingston, Aarno Palotie, David B Savage, Mark O'DriscollMark O'Driscoll, Claire Smith, Stephen O'Rahilly, Inês Barroso, Robert K Semple
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History

Publication status

  • Published

Journal

Frontiers in Genomic Endocrinology

Issue

Articl

Volume

2

Department affiliated with

  • Sussex Centre for Genome Damage Stability Publications

Notes

This was the first article to be published in the inaugural issue of this journal.

Full text available

  • No

Peer reviewed?

  • Yes

Legacy Posted Date

2012-02-06

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