Taxon:

Human

Gene:

9p22-pter phenotype

Chromosome:

09

Location:

9p22-pter

Description:

Deletion of the paternally derived chromosome 9 (p22-pter) was associated with minimal dysmorphic stigmata (usually 9p deletion is associated with distinctive features). The authors hypothesise that imprinting may influence the phenotype (Kleczkowska A et al, 1992).

Category:

Disomy (UPD)

Record:

131

Last Modified 4/27/2010

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