Fig. 4From: Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutationsFull mutation occurrence in the family. Figure 4. shows the case of family No.15 (code 436), showing the Southern blot image in addition to the RP-PCR results. The patient (436/5) inherited the paternal 87 CGG premutation allele, the 89 CGG repeat showed a low repeat number expansion. There were two cases of full mutation form with the Fragile X syndrome in the familyBack to article page