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Microcephaly, holoprosencephaly, hypokinesia--second report of a new syndrome.

作者信息

Hockey A, Crowhurst J, Cullity G

机构信息

Department of Clinical Genetics, King Edward Memorial Hospital, Perth, Western Australia.

出版信息

Prenat Diagn. 1988 Nov;8(9):683-6. doi: 10.1002/pd.1970080909.

Abstract

Two still-born males whose mothers were sisters are presented. The features holoprosencephaly, hypokinesia, microcephaly, talipes, and other contractures correspond to those in the two male sibs reported by Morse et al. (1987). We suggest that our cases now provide evidence of an X-linked rather than an autosomal recessive new syndrome.

摘要

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