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RSS FeedsA chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family (Molecular Cytogenetics)

 
 

4 june 2020 18:10:57

 
A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family (Molecular Cytogenetics)
 


Copy number variants (CNVs) associated with developmental delay and intellectual disability (DD/ID) continue to be identified in patients. This article reports identification of a chromosome 1q22 microdeletion...


 
70 viewsCategory: Biotechnology, Genetics, Molecular Biology
 
Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder (Molecular Cytogenetics)
 
 
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