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Article

Familial interstitial deletion 11(p11.12p12) associated with parietal foramina, brachymicrocephaly, and mental retardation

1 Mar 1993

Abstract excerpt

Parietal foramina may be an isolated autosomal dominant trait or found in syndromes. We report on two related individuals who have multiple anomalies with parietal foramina and the deletion of 11(p11.12p12) due to the inheritance of a derivative chromosome 11 from an insertional translocation dir ins (13;11)(q14.1; p11.12p12). Results of initial chromosome analyses on the proposita and her maternal half-uncle...

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Identifiers

PMID: 8456828
DOI: 10.1002/ajmg.1320450512

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Source receipt: pubmed, retrieved 7 Sept 2026.

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