Fig. 3From: Human AZFb deletions cause distinct testicular pathologies depending on their extensions in Yq11 and the Y haplogroup: new cases and review of literaturea Schematic view on extensive map of genomic STS markers flanking the AZFb Y genes in the AZFb interval of the human Y chromosome to distinguish the extension of partial AZFb deletions of patients with distinct testicular pathologies. b The SNV deletion map of these patients for the distal AZFb-AZFc overlap region at the right is presented in Table 2 and therefore only partly viewed here in this schemeBack to article page