Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing pbx1 gene

HIGHLIGHTS

• who: Man Luo from the (UNIVERSITY) have published the research work: Prenatal diagnosis and molecular cytogenetic analyses of a paternal inherited deletion of 1q23.3 encompassing PBX1 gene, in the Journal: (JOURNAL) of 13/Dec/2022
• what: The authors provide a detailed description of the phenotype in a family with paternal inherited deletion of 1q23.3 encompassing exons 1-2 of the PBX1 gene.
• future: More studies is needed to provide further insights into the pathogenesis of 1q23.3 deletion.

SUMMARY

The incidence of chromosome 1q deletion in the . . .

 



If you want to have access to all the content you need to log in!

Thanks :)

Username or Email

Password

Remember me

Lost your password?

If you don't have an account, you can create one here.