Skip to main content

Advertisement

Fig. 2 | BMC Medical Genetics

Fig. 2

From: A novel frameshift mutation in FRMD7 causes X-linked infantile nystagmus in a Chinese family

Fig. 2

Pedigrees of this Chinese family. Filled symbols demonstrate affected patients and unfilled symbols demonstrate unaffected patients. The dotted circles show female carriers. Arrow indicates the proband. Red indicates that patients underwent a genetic test and partial clinical examination. Blue indicates that patients underwent a genetic test and complete clinical examination

Back to article page