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Fig. 1 | BMC Medical Genetics

Fig. 1

From: NSDHL-containing duplication at Xq28 in a male patient with autism spectrum disorder: a case report

Fig. 1

a Photographs of P01. P01 represents the patient. Minor facial anomalies include a depressed nasal bridge and thick, drooping upper eyelids. b Pedigree of family P01. Standard pedigree symbols are used. P01 represents the patient, P02 represents the mother of the patient, and P03 represents the father. c Confirmation of results using real-time qPCR. Ctrl M and Ctrl F are male and female controls with normal NSDHL gene dosage/expressions. P01 represents the patient, P02 represents the mother of the patient, and P03 represents the father of the patient. The crossing point (CP) values of each sample were normalized to that of a housekeeping gene, MPO/GAPDH. Error bars denote the standard deviation for five DNA/RNA samples. All data are shown as the mean ± SEM. P01 had inherited the NSDHL duplication from P02, and P03 carried a normal sequence

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