Fig. 5From: C-banding and AgNOR-staining were still effective complementary methods to indentify chromosomal heteromorphisms and some structural abnormalities in prenatal diagnosisPrenatal diagnosis of 45,X [31]/46,X,r(X)(p11;q21) [29] in Case #3. Abnormal chromosome is indicated by arrows. (a) G-banding Karyotype. (b) C-banding Karyotype . (c) CNV-seq analysis revealed large fragment deletions in chromosome X deletion. The gray baseline beside the chromosome represent the copy number of chromosomes was normal, green portions of the baseline represented the regions in chromosome were deletionsBack to article page