Pathogenic variants in the paired-related homeobox 1 gene (PRRX1) cause craniosynostosis with incomplete penetrance

Authors :: Tooze, R.
Miller, K.A.
Swagemakers, S.M.A.
Calpena, E.
McGowan, Simon J.
Boute, Odile
Leeuw, N. de
Ockeloen, Charlotte W.
Twigg, S.R.F.
Wilkie, Andrew O. M.
Tooze, R.
Miller, K.A.
Swagemakers, S.M.A.
Calpena, E.
McGowan, Simon J.
Boute, Odile
Leeuw, N. de
Ockeloen, Charlotte W.
Twigg, S.R.F.
Wilkie, Andrew O. M.
Source :: Genetics in Medicine; 1098-3600; 9; 25; 100883; ~Genetics in Medicine~~~~~1098-3600~9~25~~100883
Publication Year :: 2023
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: Genetics in Medicine; 1098-3600; 9; 25; 100883; ~Genetics in Medicine~~~~~1098-3600~9~25~~100883
Publication Type :: Electronic Resource
Accession number :: edsoai.on1396122685
Document Type :: Electronic Resource

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