Acute Pre-B Lymphoblastic Leukemia and Congenital Anomalies in a Child with a de Novo 22q11.1q11.22 Duplication

Microdeletions and microduplications are recurrent in the q11.2 region of chromosome 22. The 22q11.2 duplication syndrome is an extremely variable disorder with a phenotype ranging from severe intellectual disability, facial dysmorphism, heart defects, and urogenital abnormalities to very mild sympt...

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Detalles Bibliográficos
Autores principales: Vaisvilas, M, Dirse, V, Aleksiuniene, B, Tamuliene, I, Cimbalistiene, L, Utkus, A, Rascon, J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231321/
https://www.ncbi.nlm.nih.gov/pubmed/30425917
http://dx.doi.org/10.2478/bjmg-2018-0002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231321/
https://www.ncbi.nlm.nih.gov/pubmed/30425917
http://dx.doi.org/10.2478/bjmg-2018-0002

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