Literature DB >> 33758130

6p21.33 Deletion encompassing CSNK2B is associated with relative macrocephaly, facial dysmorphism, and mild intellectual disability.

Ikuko Ohashi1, Yukiko Kuroda1, Yumi Enomoto2, Hiroaki Murakami1, Mitsuo Masuno3, Kenji Kurosawa1,2.   

Abstract

Entities:  

Year:  2021        PMID： 33758130     DOI： 10.1097/MCD.0000000000000372

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  1 in total

1.  Two different presentations of de novo variants of CSNK2B: two case reports.

Authors:  Matheus V M B Wilke; Bibiana M Oliveira; Alessandra Pereira; Maria Juliana R Doriqui; Fernando Kok; Carolina F M Souza
Journal:  J Med Case Rep       Date:  2022-01-05
  1 in total

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