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RSS FeedsA case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability (BMC Medical Genomics)

 
 

16 april 2020 19:03:16

 
A case report of familial 4q13.3 microdeletion in three individuals with syndromic intellectual disability (BMC Medical Genomics)
 


Interstitial 4q deletions are rare chromosomal alterations. Most of the previously reported deletions involving the 4q13.3 region are large chromosomal alterations with a common loss of band 4q21 resulting in ...


 
237 viewsCategory: Genomics, Medicine
 
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