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Article

Recurrent Wiedemann‐Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)

15 Feb 1992

Abstract excerpt

A baby with Wiedemann-Beckwith syndrome (WBS) and her phenotypically normal mother carried the same paracentric inversion, inv(11)(p11.2 15.5), in the short arm of chromosome 11. A fetus, sib of the affected baby, had the same inversion and ultrasound scan showed exomphalos. The maternal grandmother is clinically and cytogenetically normal. The pattern of affection in this family is consistent with the suggestion...

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Identifiers

PMID: 1609847
DOI: 10.1002/ajmg.1320420441

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