Volume 39, Issue 2 pp. 142-148
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Trisomy 18 and 18p- features in a case of isochromosome 18q [46,XY,i(18q)]: prenatal diagnosis and autopsy report

Doris H. Wurster-Hill

Corresponding Author

Doris H. Wurster-Hill

Department of Pathology, Dartmouth-Hitchcock Medical Center, Hanover, N.H., U.S.A.

Department of Pathology Dartmouth-Hitchcock Medical Center Hanover, New Hampshire 03756 U.S.A.Search for more papers by this author
J. Miguel Marin-Padilla

J. Miguel Marin-Padilla

Department of Pathology, Dartmouth-Hitchcock Medical Center, Hanover, N.H., U.S.A.

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John B. Moeschler

John B. Moeschler

Department of Maternal and Child Health, Dartmouth-Hitchcock Medical Center, Hanover, N.H., U.S.A.

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Jonathan P. Park

Jonathan P. Park

Department of Pathology, Dartmouth-Hitchcock Medical Center, Hanover, N.H., U.S.A.

Department of Biological Sciences, Dartmouth College, Hanover, N.H., U.S.A.

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Melanie McDermet

Melanie McDermet

Department of Maternal and Child Health, Dartmouth-Hitchcock Medical Center, Hanover, N.H., U.S.A.

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First published: February 1991
Citations: 11

Abstract

This paper reports the prenatal diagnosis and autopsy findings of a case of true isochromosome 18q [46,XY,i(18q)] with severe cephalic malformations. Comparison is made with other cases of i(18q).

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