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Fig. 3 | Cell & Bioscience

Fig. 3

From: Human AZFb deletions cause distinct testicular pathologies depending on their extensions in Yq11 and the Y haplogroup: new cases and review of literature

Fig. 3

a 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 scheme

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