Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334kb deletion: A case report

Author:                      

Publisher: Spandidos Publications

ISSN: 1791-2997

Source: Molecular Medicine Reports, Vol.9, Iss.1, 2014-01, pp. : 163-165

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next