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Fig. 1 | Human Genomics

Fig. 1

From: The significance of trisomy 7 mosaicism in noninvasive prenatal screening

Fig. 1

NIPT and CMA results for case 22 and karyotype results for the parents of case 22. a NIPT result for case 22. Chr7: dup (90 M–157 M); chrX: del (0.1 M–52 M). b CMA result for case 22. The chromosomal regions in the red mark were the missing pieces of that deletion at the position of 7q21.13q36.3(89,040,945-159,119,707), and the blue marks are the missing pieces at the position of Xp22.33p11.22(168,551-53,973,336). c Karyotype results for the parents of case 22 were normal

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