X-linked laterality sequence in a family with carrier manifestations.
作者信息
Mikkilä S P, Janas M, Karikoski R, Tarkkila T, Simola K O
机构信息
Department of Clinical Genetics, Tampere University Hospital, Finland.
出版信息
Am J Med Genet. 1994 Feb 15;49(4):435-8. doi: 10.1002/ajmg.1320490417.
PMID:8160739
Abstract
X-linked laterality sequence (XLLS) consists of situs inversus, complex cardiac defects, and alterations in the development of the spleen. We describe a family in which two male cousins had XLLS with caudal manifestations. In our family, the obligate carrier females had uterine septum and hypertelorism, which may be gene carrier manifestations.
摘要
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