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Using comprehensive genomic and functional analyses for resolving genotype–phenotype mismatches in children with suspected CMMRD in Lebanon: an IRRDC study

Crossref DOI link: https://doi.org/10.1007/s00439-023-02530-8

Published Online: 2023-02-15

Published Print: 2023-04

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Hamideh, Dima

Das, Anirban

Bianchi, Vanessa

Chung, Jiil

Negm, Logine

Levine, Adrian

Basbous, Maya

Sanchez-Ramirez, Santiago

Mikael, Leonie

Jabado, Nada

Atweh, Lamya

Lteif, Mireille

Mahfouz, Rami

Tarek, Nidale

Abboud, Miguel

Muwakkit, Samar

Hawkins, Cynthia

Tabori, Uri

Saab, Raya https://orcid.org/0000-0001-5776-2303
,
Funding

Funding for this research was provided by:

Hospital for Sick Children

Stand Up To Cancer Canada

St. Baldrick's Foundation
License Information

Text and Data Mining valid from 2023-02-15

Version of Record valid from 2023-02-15
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Article History

Received: 12 September 2022

Accepted: 4 February 2023

First Online: 15 February 2023

Declarations

:

: The authors declare that they have no conflict of interest.

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