Volume 44, Issue 6 pp. 335-337
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De novo interstitial deletion of the long arm of chromosome 3:46, XX, del(3) (q25.1q26.1)

Nathaniel H. Robin

Corresponding Author

Nathaniel H. Robin

Division of Human Genetics, Children's Hospital of Philadelphia, USA

M.D., Division of Human Genetics, Children's Hospital of Philadelphia, 34th and Civic Center Blvd., Philadelphia, Pa. 19104, USASearch for more papers by this author
Mark Magnusson

Mark Magnusson

Diagnostic Center, Children's Hospital of Philadelphia, USA

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Donna McDonald-McGinn

Donna McDonald-McGinn

Division of Human Genetics, Children's Hospital of Philadelphia, USA

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Elaine H. Zackai

Elaine H. Zackai

Division of Human Genetics, Children's Hospital of Philadelphia, USA

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Nancy B. Spinner

Nancy B. Spinner

Division of Human Genetics, Children's Hospital of Philadelphia, USA

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First published: December 1993
Citations: 8

Abstract

Robin NH, Magnusson M, McDonald-McGinn D, Zackai EH, Spinner NB. De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3) (q25.1q26.1). Clin Genet 1993: 44: 335–337. © Munksgaard, 1993

A girl with an interstitial deletion of chromosome 3 is presented. The facial resemblance to an earlier reported patient with a shared breakpoint is addressed.

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