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A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome |
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Titel: |
A novel MEIS2 mutation explains the complex phenotype in a boy with a typical NF1 microdeletion syndrome |
Auteur: |
Santoro, Claudia Riccio, Simona Palladino, Federica Aliberti, Ferdinando Carotenuto, Marco Zanobio, Mariateresa Peduto, Cristina Nigro, Vincenzo Perrotta, Silverio Piluso, Giulio |
Verschenen in: |
European journal of medical genetics |
Paginering: |
Jaargang 64 () nr. 5 pagina's p. |
Jaar: |
2021 |
Inhoud: |
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Uitgever: |
Elsevier Masson SAS |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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