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                                       Details for article 31 of 939 found articles
 
 
  O36: Long-read genome sequencing in unsolved rare genetic diseases: Preliminary experiences from the Care4Rare Canada Consortium
 
 
Title: O36: Long-read genome sequencing in unsolved rare genetic diseases: Preliminary experiences from the Care4Rare Canada Consortium
Author: Del Gobbo, Giulia
Couse, Madeline
Lambert, Christine
Zhang, Siyuan
Dhillon, Harsharan
Fanslow, Cairbre
Rowell, William
Dolzhenko, Egor
De Sena Brandine, Guilherme
Eberle, Michael
Marshall, Christian
Kernohan, Kristin
Boycott, Kym
Appeared in: Genetics in medicine open
Paging: Volume 2 () nr. S1 pages p.
Year: 2024
Contents:
Publisher: Published by Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 31 of 939 found articles
 
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