Lobar holoprosencephaly and Xq22 deletion.

  • 1 January 1991
    • journal article
    • Vol. 2  (2) , 119-21
Abstract
A 20 weeks gestation female fetus with a lobar holoprosencephaly and Xq22 deletion is described. The phenotype correlation of the cerebral defect with the facial features is positive. On the contrary phenotypic-karyotypic correlation is non obvious.

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