Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality
Keywords: کروموزوم 4; 5q13.2 microdeletion; chromosome 4; mosaicism; prenatal diagnosis; small supernumerary marker chromosome;