
Prenatal diagnosis of pure partial monosomy 18p associated with holoprosencephaly and congenital heart defects
Keywords: نقص مادرزادی قلب; CMA, Chromosome Microarray Analysis; HPE, holoprosencephaly; FISH, fluorescent in situ hybridizationMonosomy 18p; Microarray analysis; Genotype–phenotype correlation; Prenatal diagnosis; Holoprosencephaly; Congenital heart defects