A most unusual phenotype in a patient with a mosaic ASXL1 deletion

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Bibliographic Details
Published in:European journal of human genetics : EJHG 2023-05, Vol.31 (Supplément 1)
Main Authors: Destrez, Alban, Jedraszak, Guillaume, Fritot, Séverine, Gondry-Jouet, Catherine, Bryselbout, Sophie, Marie-Christine, Plancq, Gbaguidi, Cica, Demeer, Bénédicte
Format: Article
Language:English
Subjects:
Biochemistry, Molecular Biology
Genetics
Human genetics
Life Sciences
Online Access:Get full text
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ISSN:1018-4813
1476-5438