Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance
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Published:2023-09
Issue:9
Volume:25
Page:100883
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
Tooze Rebecca S.ORCID,
Miller Kerry A.,
Swagemakers Sigrid M.A.,
Calpena Eduardo,
McGowan Simon J.,
Boute Odile,
Collet Corinne,
Johnson David,
Laffargue Fanny,
de Leeuw Nicole,
Morton Jenny V.,
Noons Peter,
Ockeloen Charlotte W.,
Phipps Julie M.,
Tan Tiong Yang,
Timberlake Andrew T.,
Vanlerberghe Clemence,
Wall Steven A.,
Weber Astrid,
Wilson Louise C.,
Zackai Elaine H.,
Mathijssen Irene M.J.,
Twigg Stephen R.F.ORCID,
Wilkie Andrew O.M.ORCID
Subject
Genetics (clinical)
Cited by
4 articles.
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