期刊
CLINICAL CASE REPORTS
卷 4, 期 10, 页码 968-971出版社
WILEY
DOI: 10.1002/ccr3.669
关键词
10p15.3 deletion; familial microcephaly; neurodevelopmental delays
A focused genetic workup is useful in determining the cause of familial microcephaly, especially in the setting of mildly different phenotypes. As illustrated by this case from an impoverished international urban location, one must not assume the etiology for the apparent familial microcephaly is the same for all affected members.
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