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Fig. 1 | BMC Endocrine Disorders

Fig. 1

From: A case of familial central precocious puberty caused by a novel mutation in the makorin RING finger protein 3 gene

Fig. 1

Pedigree of the family with the novel mutation of MKRN3 gene. Squares indicate male family members. Circles indicate females. Black symbols indicate patients with CPP and, in case of the grandmother, with precocious menarche. Symbol with black points inside indicate the asymptomatic carriers. White symbols indicate non mutated patients. The arrow indicates the proband

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