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Fig. 1 | Molecular Cytogenetics

Fig. 1

From: Clinical application of chromosomal microarray analysis for fetuses with craniofacial malformations

Fig. 1

Abnormal ultrasonographic findings and the identified pCNVs of three selected fetuses. a A 0.96ā€‰Mb deletion related to 22q11.2 distal deletion syndrome (A2) was identified in fetus 17 with cleft lip (A1). b A 1.20ā€‰Mb deletion of 6p25.3p25.2 (B2) was identified in fetus 32 with hypertelorism (B1). c A 0.44ā€‰Mb deletion of 1q21.11q21.2 (C2) was identified in fetus 33 with micrognathia (C1)

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