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Fig. 4 | BMC Medical Genetics

Fig. 4

From: Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations

Fig. 4

Full 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 family

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BMC Medical Genetics

ISSN: 1471-2350

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