Objective: To report a rare family of AZFc deletion with natural transmission and explore the potential mechanism by which identical microdeletions cause different phenotypes.
目的：报告1个父子间AZFc缺失自然遗传的罕见家系，探讨该家系相同缺失类型导致不同临床表型的可能机制。
Objective: To report a rare family of AZFc deletion with natural transmission and explore the potential mechanism by which identical microdeletions cause different phenotypes.
目的：报告1个父子间AZFc缺失自然遗传的罕见家系，探讨该家系相同缺失类型导致不同临床表型的可能机制。
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