Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association.

Kumar, Jeevan M

Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic association. [electronic resource] - Indian journal of human genetics Sep 2011 - 241-3 p. digital

Publication Type: Case Reports; Journal Article

0971-6866

10.4103/0971-6866.92089 doi