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A Novel Mutation Of The RPGRIP1L Gene In A Chinese Boy With Joubert Syndrome With Oculorenal Involvement
This is one of the pictures featuring the A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvement. Several images associated with the A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvement can be utilized as your point of reference. Below, you'll find some more pictures related to the A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvement.
Title: Joubert syndrome: a rare developmental disorder of brain - medizzyJoubert syndrome: a rare developmental disorder of brain - medizzy.
Title: Genes | free full-text | exome analysis reveals novel missense andGenes | free full-text | exome analysis reveals novel missense and.
Title: (pdf) a novel mutation of the rpgrip1l gene in a chinese boy with(pdf) a novel mutation of the rpgrip1l gene in a chinese boy with.
