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RSS FeedsIdentification of a novel deletion mutation in DPY19L2 from an infertile patient with globozoospermia: a case report (Molecular Cytogenetics)

 
 

22 june 2020 21:31:43

 
Identification of a novel deletion mutation in DPY19L2 from an infertile patient with globozoospermia: a case report (Molecular Cytogenetics)
 


Male infertility is an increasing medical concern worldwide. In most cases, genetic factors are considered as the main cause of the disease. Globozoospermia (MIM102530) (also known as round-headed sperm) is a ...


 
104 viewsCategory: Biotechnology, Genetics, Molecular Biology
 
Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder (Molecular Cytogenetics)
Inherited duplication of the pseudoautosomal region Xq28 in a subject with Gilles de la Tourette syndrome and intellectual disability: a case report (Molecular Cytogenetics)
 
 
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