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RSS FeedsRare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder (Molecular Cytogenetics)

 
 

10 june 2020 20:18:35

 
Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder (Molecular Cytogenetics)
 


Small supernumerary marker chromosomes (sSMCs), are additional abnormal chromosomes, which can`t be detected accurately by banding cytogenetic analysis. Abnormal phenotypes were observed in about 30% of SMC ca...


 
99 viewsCategory: Biotechnology, Genetics, Molecular Biology
 
A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family (Molecular Cytogenetics)
Identification of a novel deletion mutation in DPY19L2 from an infertile patient with globozoospermia: a case report (Molecular Cytogenetics)
 
 
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